Recombinant TNF Ligand Family Member Polypeptides with Antibody Binding Domain and Uses Thereof

ABSTRACT

The present invention relates in general to the field of TNF ligand family members. In more detail the present invention relates to polypeptides comprising at least three components A, each of which comprises the sequence of a TNF homology domain (THD) of a TNF ligand family member, or a functional derivative thereof, and comprising at least one component B consisting of a V L  region and a V H  region linked directly to each other with a linker sequence L which has a length of &lt;12 amino acids. Furthermore, the present invention also relates to nucleic acids encoding such polypeptides and pharmaceutical compositions thereof.

The present invention relates in general to the field of TNF ligand family members. In more detail the present invention relates to polypeptides comprising at least three components A, each of which comprises the sequence of a TNF homology domain (THD) of a TNF ligand family member, or a functional derivative thereof, and comprising at least one component B consisting of a V_(L) region and a V_(H) region linked directly to each other with a linker sequence L which has a length of ≦12 amino acid residues. Furthermore, the present invention also relates to nucleic acids encoding such polypeptides.

The members of the TNF ligand family are proinflammatory cytokines. Cytokines in general, and in particular the members of the TNF ligand family, play a crucial role in the stimulation and coordination of the innate immune system as well as in the adaptive immune response (including both cellular and humoral immunity), induction of apoptosis, bone architecture, hair growth, teeth growth, development of perspiratory glands, lymph node development and many more (Aggarwal, B. B. (2003), Nat. Rev. Immunol. 3, 745-756). A dysregulation of the activity of members of the TNF ligand family can, however, lead to a multitude of pathologies. This includes for example septic shock, autoimmune diseases like rheumatoid arthritis, or neurodegenerative diseases. Tumor necrosis factor (TNF) is the name-giving and probably most important member of this large cytokine family.

Members of the TNF ligand family exert their biological function as homotrimers (Banner, D. W. et al, (1993), Cell 73, 431-445). Trimeric structures and likewise aggregations of higher order (e.g. oligomers or multimers of trimers) of such proteins may be encountered frequently in nature. Examples for this are the Cartilage Matrix Protein (CMP), which is a connective tissue protein (Beck et al. (1996), J. Mol. Biol. 256, 909-923), proteins of the family of collagens, like the Clq family to which Clq, collagen α1 (X), α2 (VII), the hibernation protein, ACRP30, the inner ear structure protein, cellebrin and multimerin belong (Kishore and Reid (1999), Immunopharmacol. 42, 15-21), and proteins of the collectin family such as lung surfactant protein A (SP-A) and mannose binding protein (MBP) (Epstein et al., (1996), Current Opinion in Immunology, Vol. 8, No. 1, 29-35).

Trimer formation occurs due to interactions between the individual monomers such as hydrophobic interactions, hydrogen bridges, covalent bonds (e.g. disulfide bonds), and/or Coulomb forces, but also occurs on basis of structural motifs, i.e. specific amino acid sequences which lead to formation of intermolecular supersecondary structures. In case of the members of the TNF ligand family, the three monomers associate in the homotrimeric structure via non-covalent hydrophobic bonds. In the active form they in turn activate members of the TNF receptor family which themselves do not possess any enzymatic activity. For example, TNF being a member of the TNF ligand family binds to the two membrane receptors TNFR1 and TNFR2 and mediates the oligomerization and the activation of inactive receptors. As a consequence of the receptor complex formation a signal cascade is initiated which brings about inter alia an association of cytoplasmatic adaptor proteins (Wajant, H. et al. (2003), Cell Death, Differ, 10, 45-65). The interaction of TNFR1 and TNFR2 with its ligand is characterized by binding of the receptors at the space between two of the three TNF monomers of the TNF homotrimer (Banner (1993), supra). This illustrates that TNF as well as all the other members of the TNF ligand family are only biologically active in the homotrimeric structure. Due to their function, members of the TNF ligand family and the respective membrane receptors, respectively, may be used for many kinds of treatments of diseases, such as infectious diseases, inflammatory diseases, metabolic diseases, diseases resulting from a dysregulation of apoptosis, neurodegenerative diseases and many more diseases. They play a particularly important role in the treatment of cancerous diseases because members of the TNF ligand family exhibit in general an antitumor activity. This applies in particular to TNF (Eggermont, A. M. and ten Hagen, T. L. (2003), Curr. Oncol. Rep. 5, 79-80), TRAIL (TNF related apoptosis using ligand), also termed Apo 2L (Weley et al. (1995), Immunity 6: 673-682; Petti et al. (1996), J. Biol. Chem. 271: 12687-12689) and FasL (CD95L). However, in vivo experiments showed strong systematic adverse reactions for TNF and agonists of the Fas receptor, and in vitro experiments indicate similarly toxic effects for certain TRAIL compounds (Jo et al. (2000) Nat Med 6: 564-567, Ichikawa et al. (2001) Nat Med 7: 954-960; Ogasawara et al. (1993) Nature 364: 806-809). For this reason, the clinical use of Fas activating ligands/agonists in a systemic application has so far been considered impossible due to safety concerns. However, due to the importance of TNF, TRAIL, FasL (CD95L) and other TNF ligand family members for this field, and due to the adverse reactions associated with their application in form of a clinical systemic administration, several alternative approaches were pursued in order to minimize the adverse reactions (Eggermont, A. M. and ten Hagen, T. L. (2003), Curr. Oncol. Rep. 5, 79-80).

WO 02/22680 describes for example fusion proteins which allow a targeted and tissue and/or cell-specific activity of cytokines by fusing the cytokine with an antigen-binding antibody. By this means it is achieved that the cytokine is not active on tissue or cells, respectively, which are not in contact with these fusion proteins, and that adverse reactions regarding these tissues and cells, respectively, are reduced.

In DE 102 47 755 an antibody-independent system is disclosed, which likewise allows for a targeted, tissue- and cell-specific action of the cytokines. The document discloses fusion proteins with a biologically active domain and a cell surface binding domain. Biological activity of the biologically active domain is mediated by binding of the cell surface binding domain to the respective cell surface. Besides of providing a reduction of adverse reactions for non-target tissue, this system may also be advantageously used for cell surface molecules on target cells for which no or only low specificity antibodies are available.

Apart from the above-mentioned adverse reactions it is additionally problematic that the active homotrimers of members of the TNF ligand family dissociate even at physiologically reasonable concentrations. This dissociation is reversible; however, the protein quickly loses its bioactivity because it is denaturing. It is assumed that this denaturing is due to the intermediate, unstable monomers (Smith, R. A. and Baglioni, C. (1987), J. Biol. Chem. 262, 6951-6954; Narhi, L. O. and Arakawa, T. (1987), Biochem. Biophys. Res. Commun 147, 740-746).

In a first attempt this problem has been addressed in the art for example in WO 01/25277. WO 01/25277 discloses single-chain TNFα polypeptides with 3 copies of a TNFα monomer. Due to the single chain nature, dissociation is prevented. A similar concept is disclosed in WO 2005/103077.

In addition it has been reported in the prior art that oligomeric molecules of TNF ligand family members exhibit increased activity but likewise increased toxicity (Koschny R et al. J Mol Med 2007; 85: 923-935; Gerspach J et al., Results Probl Cell Differ. 2009; 49:241-73. Review. Wyzgol et al J I 2010).

Thus, there is still in the art a need for novel and improved TNF ligand family derived compounds, which are preferably stable, exhibit few(er) or no adverse systemic reactions while in parallel maintaining biological specificity.

This object is solved by the present invention, in particular by means as set forth in the appended set of claims and as illustrated in the following.

The inventors of the present invention have surprisingly found that polypeptides of the present invention exhibit increased activity against tumors while they do at the same time surprisingly not exhibit increased toxicity towards non-tumor tissue.

Essentially, the polypeptides of the present invention are fusion proteins comprising on the one hand at least three TNF ligand family member monomers and comprising the variable domains of an antibody V_(L) and V_(H) region linked by a short linker as targeting moiety on the other hand. To increase specificity, to increase in vivo half-life and to modulate pharmacodynamic properties, the polypeptides according to the present invention may further comprise an albumin binding domain and/or other domains and/or other modifications.

Thus, in a first aspect the present invention relates to a polypeptide which comprises:

-   -   a) at least three components A, each of which comprises the         sequence of a TNF homology domain (THD) of a TNF ligand family         member, or functional derivative thereof, and     -   b) at least one component B consisting of a V_(L) region and a         V_(H) region linked directly to each other with a linker         sequence L which has a length of ≦12 amino acid residues.

The term “polypeptide” as used herein refers to a polymer composed of a sequence of amino acids. The term shall not be construed as limiting the length of the polypeptide unit. However, preferably, the polypeptide has a length of less than 1000 amino acids, more preferably less than 900 amino acids. The amino acids within the polymer of said polypeptide sequence are usually linked to each other via peptide bonds, but modifications of said peptide bond(s) or of side chain residues may be tolerable, provided the overall activity is not totally lost, e.g. the resulting chemical entity (e.g. components A) still trimerizes and activates its targets.

The TNF homology domain is the common structural feature shared by all TNF ligand family members Bodmer J L et al. (Trends Biochem Sci. 2002 January; 27(1):19-26.). It comprises the receptor binding sites and is thus critical for the biologic activity of the TNF ligand family members. A component A of the present invention may have as minimal motif the THD, e.g. of a given TNF ligand family member, but may for example also comprise longer sequence stretches of TNF ligand family members such as the sequence of the soluble form (shed or secreted, respectively) of said TNF ligand family member. The sequence may also comprise the entire extracellular domain of a TNF ligand family member, but preferably without the protease cleavage site naturally present in some of these TNF ligand family members, e.g. without a TACE/ADAM17 cleavage site in order to avoid cleavage of the fusion protein in the region comprising the three components A.

The THD domain may be for example selected from the TNF ligand family member group consisting of: FasL (CD95L), TRAIL, TNF, LT alpha, LT beta, CD30L, CD40L, OX40L, RANKL, TWEAK, LIGHT, CD27L, 4-1BBL, GITRL, APRIL, EDA 1, EDA 2, VEGI und BAFF. Particularly preferred are the human TNF ligand family members human FasL (CD95L), human TRAIL, human TNF, human LT alpha, human LT beta, human CD30L, human CD40L, human OX40L, human RANKL, human TWEAK, human LIGHT, human CD27L, human 4-1 BBL, human GITRL, human APRIL, human EDA 1, human EDA 2, human VEGI und human BAFF.

Further information, in particular about sequences of the TNF ligand family members, may be obtained for example from publicly accessible databases such as the GenBank: FasL (CD95L) (GenBank Accession No. NM_000639), TRAIL (TNF Related Apoptosis Inducing Ligand; GenBank Accession No. NM_003810), also Apo2L termed, TNF (Tumor Nekrose Faktor; GenBank Accession No. NM_000594), LT alpha (GenBank Accession No. NM_000595), Lymphotoxin beta (GenBank Accession No. NM_002341), CD30L (CD153; GenBank Accession No. NM_001244), CD40L (CD154; GenBank Accession No. NM_00074), OX40L (GenBank Accession No. NM_003326), RANKL (GenBank Accession No. NM_003701), TWEAK (GenBank Accession No. NM_003809), LIGHT (GenBank Accession No. NM_003807), CD27L (GenBank Accession No. NM_001252), 4-1 BBL (GenBank Accession No. NM_003811), GITRL (GenBank Accession No. NM_005092), APRIL (GenBank Accession No. NM_172089), EDA 1/2 (GenBank Accession No. NM_001399; NM_001005609), VEGI (GenBank Accession No. NM_005118) und BAFF (GenBank Accession No. NM_006573).

The sequences of the at least three components A of the polypeptides according to the invention may be selected independently of each other; e.g. the three components A may have the respective sequence of the same TNF ligand family member or may have the sequence of different TNF ligand family members or 2 of them may be identical while the other one differs in sequence (in terms of length and/or sequence). THD domains of different TNF ligand family members is in particular possible if the THD domain is selected from LT alpha or LT beta. Otherwise, it is particularly preferred if all three components A comprise the THD of the same TNF ligand family member. Certainly, similar considerations apply if the polypeptide according to the present invention comprises more than 3 components A. For example, the inventive polypeptide may comprise 4, 5, 6 or more components A. If the polypeptide according to the present invention comprises more than 3 components A then it is particularly preferred that the polypeptide comprises a multiple of three components A. By this means, two, three, four or more consecutively arranged trimers may be formed.

In a preferred embodiment a given component A may comprise or consist of one of the human sequences according to SEQ ID NOs.: 1-38 as indicated in Table 1 below, or functional fragments or functional derivatives thereof, which includes natural or artificial variations thereof or respective orthologs from other species. Preferred are orthologs from other mammalian species such as chimpanzee, mouse, swine, rat etc.

TABLE 1 Possible Components A AA SEQ ID Name: Position NO: Sequence TRAIL 120-281  1 QRVAAHITGTRGRSNTLSSPNSKNEKALGRK INSWESSRSGHSFLSNLHLRNGELVIHEKGFY YIYSQTYFRFQEEIKENTKNDKQMVQYIYKY TSYPDPILLMKSARNSCWSKDAEYGLYSIYQ GGIFELKENDRIFVSVTNEHLIDMDHEASFFG AFLVG TRAIL 118-281  2 GPQRVAAHITGTRGRSNTLSSPNSKNEKAL GRKINSWESSRSGHSFLSNLHLRNGELVIHEK GFYYIYSQTYFRFQEEIKENTKNDKQMVQYI YKYTSYPDPILLMKSARNSCWSKDAEYGLYSI YQGGIFELKENDRIFVSVTNEHLIDMDHEAS FFGAFLVG TRAIL 116-281  3 ERGPQRVAAHITGTRGRSNTLSSPNSKNEKA LGRKINSWESSRSGHSFLSNLHLRNGELVIHE KGFYYIYSQTYFRFQEEIKENTKNDKQMVQY IYKYTSYPDPILLMKSARNSCWSKDAEYGLYS IYQGGIFELKENDRIFVSVTNEHLIDMDHEAS FFGAFLVG TRAIL 114-281  4 VRERGPQRVAAHITGTRGRSNTLSSPNSKNE KALGRKINSWESSRSGHSFLSNLHLRNGELVI HEKGFYYIYSQTYFRFQEEIKENTKNDKQMV QYIYKYTSYPDPILLMKSARNSCWSKDAEYG LYSIYQGGIFELKENDRIFVSVTNEHLIDMDH EASFFGAFLVG TRAIL  95-281  5 TSEETISTVQEKQQNISPLVRERGPQRVAAHI TGTRGRSNTLSSPNSKNEKALGRKINSWESS RSGHSFLSNLHLRNGELVIHEKGFYYIYSQTY FRFQEEIKENTKNDKQMVQYIYKYTSYPDPIL LMKSARNSCWSKDAEYGLYSIYQGGIFELKE NDRIFVSVTNEHLIDMDHEASFFGAFLVG mouse TRAIL  99-291  6  TFQDTISTVPEKQLSTPPLPRGGRPQKVAAHI TGITRRSNSALIPISKDGKTLGQKIESWESSRK GHSFLNHVLFRNGELVIEQEGLYYIYSQTYFR FQEAEDASKMVSKDKVRTKQLVQYIYKYTSY PDPIVLMKSARNSCWSRDAEYGLYSIYQGG LFELKKNDRIFVSVTNEHLMDLDQEASFFGA FLIN FasL (CD95L) 144-281  7 RKVAHLTGKSNSRSMPLEWEDTYGIVLLSGV KYKKGGLVINETGLYFVYSKVYFRGQSCNNL PLSHKVYMRNSKYPQDLVMMEGKMMSYC TTGQMWARSSYLGAVFNLTSADHLYVNVS ELSLVNFEESQTFFGLYKL FasL (CD95L) 142-281  8 ELRKVAHLTGKSNSRSMPLEWEDTYGIVLLS GVKYKKGGLVINETGLYFVYSKVYFRGQSC NNLPLSHKVYMRNSKYPQDLVMMEGKMM SYCTTGQMWARSSYLGAVFNLTSADHLYV NVSELSLVNFEESQTFFGLYKL FasL (CD95L) 137-281  9 PPEKKELRKVAHLTGKSNSRSMPLEWEDTYG IVLLSGVKYKKGGLVINETGLYFVYSKVYFRG QSCNNLPLSHKVYMRNSKYPQDLVMMEGK MMSYCTTGQMWARSSYLGAVFNLTSADHL YVNVSELSLVNFEESQTFFGLYKL FasL (CD95L) 130-281 10 QIGHPSPPPEKKELRKVAHLTGKSNSRSMPLE WEDTYGIVLLSGVKYKKGGLVINETGLYFVY SKVYFRGQSCNNLPLSHKVYMRNSKYPQDL VMMEGKMMSYCTTGQMWARSSYLGAVFN LTSADHLYVNVSELSLVNFEESQTFFGLYKL FasL (CD95L) 120-281 11 QMHTASSLEKQIGHPSPPPEKKELRKVAHLT GKSNSRSMPLEWEDTYGIVLLSGVKYKKGG LVINETGLYFVYSKVYFRGQSCNNLPLSHKV YMRNSKYPQDLVMMEGKMMSYCTTGQM WARSSYLGAVFNLTSADHLYVNVSELSLVNF EESQTFFGLYKL Mouse FasL 137-279 12 EKKEPRSVAHLTGNPHSRSIPLEWEDTYGTA (CD95L) LISGVKYKKGGLVINETGLYFVYSKVYFRGQS CNNQPLNHKVYMRNSKYPEDLVLMEEKRL NYCTTGQIWAHSSYLGAVFNLTSADHLYV NISQLSLINFEESKTFFGLYKL TNF  89-233 13 VAHVVANPQAEGQLQWLNRRANALLANG VELRDNQLVVPSEGLYLIYSQVLFKGQGCPS THVLLTHTISRIAVSYQTKVNLLSAIKSPCQRE TPEGAEAKPWYEPIYLGGVFQLEKGDRLSAEI NRPDYLDFAESGQVYFGIIAL TNF  77-233 14 VRSSSRTPSDKPVAHVVANPQAEGQLQWL NRRANALLANGVELRDNQLVVPSEGLYLIYS QVLFKGQGCPSTHVLLTHTISRIAVSYQTKV NLLSAIKSPCQRETPEGAEAKPWYEPIYLGGV FQLEKGDRLSAEINRPDYLDFAESGQVYFGII AL LT alpha  59-205 15 SNLKPAAHLIGDPSKQNSLLWRANTDRAFL QDGFSLSNNSLLVPTSGIYFVYSQVVFSGKA YSPKATSSPLYLAHEVQLFSSQYPFHVPLLSS QKMVYPGLQEPWLHSMYHGAAFQLTQGD QLSTHTDGIPHLVLSPSTVFFGAFAL LT beta  82-244 16 DLSPGLPAAHLIGAPLKGQGLGWETTKEQA FLTSGTQFSDAEGLALPQDGLYYLYCLVGYR GRAPPGGGDPQGRSVTLRSSLYRAGGAYG PGTPELLLEGAETVTPVLDPARRQGYGPLWY TSVGFGGLVQLRRGERVYVNISHPDMVDFA RGKTFFGAVMVG LT beta 86-244 17 GLPAAHLIGAPLKGQGLGWETTKEQAFLTS GTQFSDAEGLALPQDGLYYLYCLVGYRGRA PPGGGDPQGRSVTLRSSLYRAGGAYGPGTP ELLLEGAETVTPVLDPARRQGYGPLWYTSV GFGGLVQLRRGERVYVNISHPDMVDFARG KTFFGAVMVG CD30L  97-234 18 KSWAYLQVAKHLNKTKLSWNKDGILHGVR YQDGNLVIQFPGLYFIICQLQFLVQCPNNS VDLKLELLINKHIKKQALVTVCESGMQTKHV YQNLSQFLLDYLQVNTTISVNVDTFQYIDTS TFPLENVLSIFLYSNSD CD30L 102-234 19 LQVAKHLNKTKLSWNKDGILHGVRYQDG NLVIQFPGLYFIICQLQFLVQCPNNSVDLKLE LLINKHIKKQALVTVCESGMQTKHVYQNLS QFLLDYLQVNTTISVNVDTFQYIDTSTFPLEN VLSIFLYSNSD CD40L 116-261 20 GDQNPQIAAHVISEASSKTTSVLQWAEKGY YTMSNNLVTLENGKQLTVKRQGLYYIYAQV TFCSNREASSQAPFIASLCLKSPGRFERILLRA ANTHSSAKPCGQQSIHLGGVFELQPGASVF VNVTDPSQVSHGTGFTSFGLLKL CD40L 113-261 21 MQKGDQNPQIAAHVISEASSKTTSVLQWAE KGYYTMSNNLVTLENGKQLTVKRQGLYYIY AQVTFCSNREASSQAPFIASLCLKSPGRFERIL LRAANTHSSAKPCGQQSIHLGGVFELQPGA SVFVNVTDPSQVSHGTGFTSFGLLKL OX40L  52-183 22 VSHRYPRIQSIKVQFTEYKKEKGFILTSQKEDE IMKVQNNSVIINCDGFYLISLKGYFSQEVNIS LHYQKDEEPLFQLKKVRSVNSLMVASLTYKD KVYLNVTTDNTSLDDFHVNGGELILIHQNP GEFCVL OX40L  55-183 23 RYPRIQSIKVQFTEYKKEKGFILTSQKEDEIMK VQNNSVIINCDGFYLISLKGYFSQEVNISLHY QKDEEPLFQLKKVRSVNSLMVASLTYKDKVY LNVTTDNTSLDDFHVNGGELILIHQNPGEF CVL RANKL 161-317 24 EAQPFAHLTINATDIPSGSHKVSLSSWYHDR GWAKISNMTFSNGKLIVNQDGFYYLYANIC FRHHETSGDLATEYLQLMVYVTKTSIKIPSSH TLMKGGSTKYWSGNSEFHFYSINVGGFFKL RSGEEISIEVSNPSLLDPDQDATYFGAFKVRD ID RANKL 140-317 25 IRAEKAMVDGSWLDLAKRSKLEAQPFAHLTI NATDIPSGSHKVSLSSWYHDRGWAKISNMT FSNGKLIVNQDGFYYLYANICFRHHETSGDL ATEYLQLMVYVTKTSIKIPSSHTLMKGGSTKY WSGNSEFHFYSINVGGFFKLRSGEEISIEVSNP SLLDPDQDATYFGAFKVRDID TWEAK 94-249 26 SAPKGRKTRARRAIAAHYEVHPRPGQDGA QAGVDGTVSGWEEARINSSSPLRYNRQIGE FIVTRAGLYYLYCQVHFDEGKAVYLKLDLLV DGVLALRCLEEFSATAASSLGPQLRLCQVSG LLALRPGSSLRIRTLPWAHLKAAPFLTYFGLF QVH TWEAK 105-249 27 RAIAAHYEVHPRPGQDGAQAGVDGTVSG WEEARINSSSPLRYNRQIGEFIVTRAGLYYLY CQVHFDEGKAVYLKLDLLVDGVLALRCLEEF SATAASSLGPQLRLCQVSGLLALRPGSSLRIR TLPWAHLKAAPFLTYFGLFQVH LIGHT  83-240 28 LIQERRSHEVNPAAHLTGANSSLTGSGGPLL WETQLGLAFLRGLSYHDGALVVTKAGYYYI YSKVQLGGVGCPLGLASTITHGLYKRTPRYP EELELLVSQQSPCGRATSSSRVWWDSSFLGG VVHLEAGEKVVVRVLDERLVRLRDGTRSYF GAFMV CD27L  51-193 29 ESLGWDVAELQLNHTGPQQDPRLYWQGG PALGRSFLHGPELDKGQLRIHRDGIYMVHI QVTLAICSSTTASRHHPTTLAVGICSPASRSIS LLRLSFHQGCTIASQRLTPLARGDTLCTNLT GTLLPSRNTDETFFGVQWVRP CD27L  56-193 30 DVAELQLNHTGPQQDPRLYWQGGPALGR SFLHGPELDKGQLRIHRDGIYMVHIQVTLAI CSSTTASRHHPTTLAVGICSPASRSISLLRLSF HQGCTIASQRLTPLARGDTLCTNLTGTLLPS RNTDETFFGVQWVRP 4-1 BBL  85-254 31 LDLRQGMFAQLVAQNVLLIDGPLSWYSDP GLAGVSLTGGLSYKEDTKELVVAKAGVYYVF FQLELRRVVAGEGSGSVSLALHLQPLRSAAG AAALALTVDLPPASSEARNSAFGFQGRLLHL SAGQRLGVHLHTEARARHAWQLTQGATV LGLFRVTPEIPAGLPSPRSE GITRL  50-177 32 QLETAKEPCMAKFGPLPSKWQMASSEPPCV NKVSDWKLEILQNGLYLIYGQVAPNANYN DVAPFEVRLYKNKDMIQTLTNKSKIQNVGG TYELHVGDTIDLIFNSEHQVLKNNTYWGIILL ANPQFIS APRIL 112-250 33 KKQHSVLHLVPINATSKDDSDVTEVMWQP ALRRGRGLQAQGYGVRIQDAGVYLLYSQV LFQDVTFTMGQVVSREGQGRQETLFRCIRS MPSHPDRAYNSCYSAGVFHLHQGDILSVIIP RARAKLNLSPHGTFLGFVKL EDA-1 245-391 34 ENQPAVVHLQGQGSAIQVKNDLSGGVLN DWSRITMNPKVFKLHPRSGELEVLVDGTYFI YSQVEVYYINFTDFASYEVVVDEKPFLQCTRS IETGKTNYNTCYTAGVCLLKARQKIAVKMV HADISINMSKHTTFFGAIRLGEAPAS EDA-2 245-389 35 ENQPAVVHLQGQGSAIQVKNDLSGGVLN DWSRITMNPKVFKLHPRSGELEVLVDGTYFI YSQVYYINFTDFASYEVVVDEKPFLQCTRSIE TGKTNYNTCYTAGVCLLKARQKIAVKMVH ADISINMSKHTTFFGAIRLGEAPAS VEGI 72-251 36 LKGQEFAPSHQQVYAPLRADGDKPRAHLT VVRQTPTQHFKNQFPALHWEHELGLAFTK NRMNYTNKFLLIPESGDYFIYSQVTFRGMTS ECSEIRQAGRPNKPDSITVVITKVTDSYPEPT QLLMGTKSVCEVGSNWFQPIYLGAMFSLQE GDKLMVNVSDISLVDYTKEDKTFFGAFLL VEGI 93-251 37 DKPRAHLTVVRQTPTQHFKNQFPALHWEH ELGLAFTKNRMNYTNKFLLIPESGDYFIYSQV TFRGMTSECSEIRQAGRPNKPDSITVVITKVT DSYPEPTQLLMGTKSVCEVGSNWFQPIYLG AMFSLQEGDKLMVNVSDISLVDYTKEDKTFF GAFLL BAFF 134-285 38 AVQGPEETVTQDCLQLIADSETPTIQKGSYT FVPWLLSFKRGSALEEKENKILVKETGYFFIYG QVLYTDKTYAMGHLIQRKKVHVFGDELSLV TLFRCIQNMPETLPNNSCYSAGIAKLEEGDEL QLAIPRENAQISLDGDVTFFGALKLL

The column “Amino acid position” indicates the amino acid residues in the full length native protein, i.e. the sequence given in the sequence column corresponds to the respective amino acid residues in the full length sequence. For example, SEQ ID NO: 1 corresponds to amino acid residues 120-281 of full length human TRAIL.

Information about natural variations of SEQ ID NOs: 1-38 and respective orthologs from other species may be easily obtained from publicly accessible databases comprising information about proteins of the TNF ligand family members or respective nucleic acid sequences. Examples for such databases are UniProt; SwissProt, TrEMBL, Protein Information Resource (PIR); Genbank, EMBL-Bank; DNA data bank of Japan (DDBJ) etc. Orthologs of other species may in particular be likewise identified via e.g. BLAST searches on basis of the respective SEQ ID NOs: 1-38.

Preferred substitutions in human TRAIL in this regard affect at least one of the following amino acids of human TRAIL: R130, G160, Y189, R191, Q193, E195, N199, K201, Y213, T214, S215, H264, 1266, D267, D269. Preferred amino acid substitutions of human TRAIL are at least one of the following substitutions: R130E, G160M, Y189A, Y189Q, R191K, Q193S, Q193R, E195R, N199V, N199R, K201R, Y213W, T214R, S215D, H264R, 1266L, D267Q, D269H, D269R, or D269K. Double or multiple substitutions are also possible, e.g. Y213W/S215D; E195R/D269H, T214R/D269H; Q193S/N199V/K201R/Y213W/S215D. Functional mutants of TRAIL are for example described in R. F. Kelley et al. (J. Biol. Chem.; 280 (2005) 2205-2212) M. MacFarlane et al. (Cancer Res 65 (2005) 11265-11270), A. M. van der Sloot et al. (Proc. Natl. Acad. Sci. USA 103 (2006) 8634-8639), V. Tur et al. (J. Biol. Chem. 283 (2008) 20560-20568), and Gasparian et al. (Apoptosis 14 (2009) 778-787). Functional mutants of TRAIL are in particular TRAIL (96-281), TRAIL (96-281)-Y189N/R191K/Q193R/H264R/1266L/D267Q, TRAIL (96-281)-Y189A/Q193S/N199V/K201/Y213W/S215D, TRAIL (96-281)-Q193S/N199V/K201R/Y213W/S215N, TRAIL (96-281)-Y189Q/R191K/Q193R/H264R/I266L/D267Q, TRAIL (114-281), TRAIL (114-281)-D269H/E195R, TRAIL (114-281)-D269H, TRAIL (114-281)-D218H, TRAIL (114-281)-D218Y, TRAIL (114-281)-Y189A/Q193S/N199V/K201/Y213W/S215D, TRAIL (114-281)-Y189N/R191K/Q193R/H264R/I266LD267Q, TRAIL (114-281)-Y189N/R191K/Q193R/H264R/I266L/D267Q/D269H, and TRAIL (114-281)-Y189N/R191K/Q193R/H264R/I266L/D269H.

As mentioned above, a component A as used herein refers to a polypeptide comprising the sequence of a TNF homology domain (THD); or a functional derivative thereof. Since the polypeptides of the present invention comprise three of said components A, trimer formation and thus the formation of the active conformation is possible. A polypeptide according to the present invention furthermore exhibits due to the presence of the at least 3 components A binding activity for the binding partners of TNF ligand family members, such as membrane-bound receptors. Functional derivatives of the TNF ligand family member sequence may exhibit (slightly) different activities and biological functions, e.g. regarding specificity or selectivity, but their overall biological function is maintained. In particular, the receptor binding activity should be maintained.

In the prior art, a multitude of methods is disclosed which allow the assessment of the biological activity of a protein, polypeptide or other molecule, respectively. Examples are protein analytical methods such as Immunoblot, ELISA, Radioimmunoassay, Immune precipitation, Surface Plasmon Resonance (Biacore), Quartz Crystal Microbalance (QCM); cell and tissue analytical methods such as immunocytochemistry, immunohistochemistry, fluorescence microscopy, FACS; cell function assays: such as cytokine-release assays, proliferation and cell cycle assays (³H-thymidine incorporation, CFSE staining), cytotoxicity assays, apoptosis assays, NFkB bandshift (EMSA) and reporter gene (Luciferase) assays, kinase assays (e.g. in Antibodies: a laboratory manual. Harlow & Lane, Cold Spring Harbor Laboratory Press; 1 edition (Dec. 1, 1988) Current Protocols in Immunology, Wiley and Sons, 1992); Cell Biology, A Laboratory Handbook 3rd ed., J Celis et al, eds. Elsevier, 2006). By this means a person skilled in the art will readily be able to assess whether a functional fragment or functional derivative of the soluble TNF ligand family member sequence retains the overall properties of the soluble TNF ligand family member (e.g. induction of apoptosis/cell death or activation of NFkB).

The term “derivative”, e.g. a functional derivative of the THD sequence or of one of the sequences according to SEQ ID NOs.: 1-38, is intended to refer also to sequences which exhibit a functional and structural similarity to the respective reference sequence. In particular the respective derivative will preferably exhibit a sequence identity of at least 50%, more preferably at least 60%, more preferably at least 70%, more preferably at least 80%, more preferably at least 85%, more preferably at least 90%, more preferably at least 92%, more preferably at least 94%, more preferably at least 95%, more preferably at least 96%, more preferably at least 97%, more preferably at least 98%, and most preferably at least 99% sequence identity with the respective reference sequence. A person skilled in the art will understand that such levels of sequence identity are preferably less than 100%. The derivative sequence and the reference sequence may differ from each other in terms of one or more insertions, deletions and/or substitutions.

As used herein, the term “% sequence identity”, has to be understood as follows: Two sequences to be compared are aligned to give a maximum correlation between the sequences. This may include inserting “gaps” in either one or both sequences, to enhance the degree of alignment. A % identity may then be determined over the whole length of each of the sequences being compared (so-called global alignment), that is particularly suitable for sequences of the same or similar length, or over shorter, defined lengths (so-called local alignment), that is more suitable for sequences of unequal length. In the above context, an amino acid sequence having a “sequence identity” of at least, for example, 95% to a query amino acid sequence, is intended to mean that the sequence of the subject amino acid sequence is identical to the query sequence except that the subject amino acid sequence may include up to five amino acid alterations per each 100 amino acids of the query amino acid sequence. In other words, to obtain an amino acid sequence having a sequence of at least 95% identity to a query amino acid sequence, up to 5% (5 of 100) of the amino acid residues in the subject sequence may be inserted or substituted with another amino acid or deleted.

Methods for comparing the identity of two or more sequences are well known in the art. The percentage to which two sequences are identical can for example be determined by using a mathematical algorithm. A preferred, but not limiting, example of a mathematical algorithm which can be used is the algorithm of Karlin et al. (1993), PNAS USA, 90:5873-5877. Such an algorithm is integrated in the BLAST family of programs, e.g. BLAST or NBLAST program (see also Altschul et al., 1990, J. Mol. Biol. 215, 403-410 or Altschul et al. (1997), Nucleic Acids Res, 25:3389-3402), accessible through the home page of the NCBI at world wide web site ncbi.nlm.nih.gov) and FASTA (Pearson (1990), Methods Enzymol. 183, 63-98; Pearson and Lipman (1988), Proc. Natl. Acad. Sci. U.S.A 85, 2444-2448). Sequences which are identical to other sequences to a certain extent can be identified by these programmes. Furthermore, programs available in the Wisconsin Sequence Analysis Package, version 9.1 (Devereux et al., 1984, Nucleic Acids Res., 387-395), for example the programs BESTFIT and GAP, may be used to determine the % identity between two polypeptide sequences. BESTFIT uses the “local homology” algorithm of (Smith and Waterman (1981), J. Mol. Biol. 147, 195-197) and finds the best single region of similarity between two sequences.

Functional derivatives in component A may in particular exhibit selective receptor binding properties, or may be optimized regarding bioactivity or other properties such as stability. In particular such derivatives may exhibit altered sequences at protease cleavage sites.

Derivatives as used herein in particular include those amino acid sequences which exhibit (for example in the context of a given level of sequence identity) in view of the respective reference sequence conservative substitutions. Conservative amino acid substitutions are preferably considered to occur within a group of amino acid residues which have sufficiently similar physicochemical properties, so that a substitution between members of the group will preserve the biological activity of the molecule (see e.g. Grantham, R. (1974), Science 185, 862-864). Particularly, conservative amino acid substitutions are preferably substitutions in which the amino acids originate from the same class of amino acids (e.g. basic amino acids, acidic amino acids, polar amino acids, amino acids with aliphatic side chains, amino acids with positively or negatively charged side chains, amino acids with aromatic groups in the side chains, amino acids the side chains of which can enter into hydrogen bridges, e.g. side chains which have a hydroxyl function, etc.). Conservative substitutions are in the present case for example substituting a basic amino acid residue (Lys, Arg, His) for another basic amino acid residue (Lys, Arg, His), substituting an aliphatic amino acid residue (Gly, Ala, Val, Leu, lie) for another aliphatic amino acid residue, substituting an aromatic amino acid residue (Phe, Tyr, Trp) for another aromatic amino acid residue, substituting threonine by serine or leucine by isoleucine. Further conservative amino acid exchanges will be known to the person skilled in the art.

Insertions, deletions and substitutions are in particular at such sequence positions possible where they do not induce a change in the three-dimensional structure or where they do not affect the binding region. A change in three-dimensional structure by means of insertions or deletions may for example be verified with CD spectral analysis (circular dichroism) (Urry 1985, Absorption, Circular Dichroism and ORD of Polypeptides, in: Modern Physical Methods in Biochemistry, Neuberger et al. (Eds.), Elsevier, Amsterdam, NL).

Suitable methods for producing derivatives of polypeptide sequences according to the present invention or components thereof, which exhibit in view of the reference sequence a substitution, are for example disclosed in U.S. Pat. No. 4,737,462, U.S. Pat. No. 4,588,585, U.S. Pat. No. 4,959,314, U.S. Pat. No. 5,116,943, U.S. Pat. No. 4,879,111 and U.S. Pat. No. 5,017,691. The production of derivatives as used herein is described in general in Maniatis et al. (2001), Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press. For this approach individual codons may simply be skipped, added or exchanged. Derivatives of polypeptide sequences mentioned herein may in particular be such polypeptide sequences which are stabilized vis-à-vis the respective reference sequence and which are less prone to physiological degradation. An example for such modification is the stabilization of the protein backbone by substitution of the amid-like bonds by using e.g. g-amino acids.

Derivatives of sequences according to the invention may in particular be produced by introducing changes into the nucleic acid sequence which encode the respective polypeptide reference sequence. Such changes may be insertions, deletions and/or substitutions of one or more nucleotides, preferably without induction of a frame shift. In the art, a multitude of methods is known for introducing such changes to nucleic acid sequences. A most common technique is the oligonucleotide-directed site-specific mutagenesis (see Comack B., Current Protocols in Molecular Biology, 8.01-8.5.9, Ausubel F. et al., 1991). Briefly, an oligonucleotide is synthesized which exhibits the sequence of a specific mutation. This oligonucleotide is then hybridized with the template (reference sequence). Preferably, this technique is used for a single-stranded template. After annealing of the modified oligonucleotide and the template, a DNA-dependent DNA polymerase is added in order to synthesize the second strand of the oligonucleotide which is complementary to the templated DNA strand. As a result, a heteroduplex molecule is formed, which comprises a mismatch, which is due to the above-mentioned mutation in the oligonucleotide. The oligonucleotide sequence is then introduced in a suitable plasmid which is in turn introduced into a suitable host cell. In the host cell the oligonucleotide is then replicated. By this means a nucleic acid sequence is obtained with specific changes (mutations) which may be used for the production of derivatives according to the present invention.

In a preferred embodiment of the present invention all and/or at least three components A of the polypeptide according to the present invention have the sequence of SEQ ID NO: 1 and/or SEQ ID NO: 5.

Preferably, the at least three components A of the polypeptides according to the present invention are linked to each other by at least two intervening peptide linkers P. In other words, two given components A within the polypeptide according to the present invention are preferably linked to each other directly via a peptide linker (e.g. A-P-A-P-A). Peptide linkers P are preferably flexible amino acid stretches and/or do not affect the intrinsic trimerization properties of the components A within the polypeptide according to the present invention. Preferably, such peptide linkers P are less than 50, even more preferably less than 45, even more preferably less than 40, even more preferably less than 35, even more preferably less than 30, even more preferably less than 25, even more preferably less than 20, even more preferably less than 15, even more preferably less than 10 amino acids long. Alternatively or in addition, the peptide linkers P have preferably an amino acid length of 1 amino acid or more, 2 amino acids or more, 3 amino acids or more, 4 amino acids or more, 5 amino acids or more, 6 amino acids or more, 7 amino acids or more, and/or 8 amino acids or more. A peptide linker linking two components A of a polypeptide of the present invention may thus have for example an amino acid length in the range of 2 to 50 amino acids, 2 to 30 amino acids, 3 to 25 amino acids, 4 to 16 amino acids, 4 to 12 amino acids or any other combination of amino acids lengths disclosed above for peptide linkers. Particularly preferred are peptide linker lengths of 1 to 8 amino acids, e.g. 4 or 8 amino acids.

In terms of amino acid sequence, the peptide linkers P linking the components A within the polypeptide of the present invention are preferably glycine (G) rich peptide linkers, i.e. are amino acid sequences with a high glycine content of more than 50%; e.g. from at least 60 to 80%, for example of about 75%. Other amino acids which may be present in the peptide linker are for example serine residues or less preferably alanine residues or glutamine residues. The peptide linker P may be composed of repetitive units. For example the linker may comprise several units of GG (SEQ ID NO: 40); GGS (SEQ ID NO: 55); GSG (SEQ ID NO: 54), or SGG (SEQ ID NO: 53) and combinations thereof. The peptide linker may also be of type which may easily be modified, e.g. glycosylated. An example for such sequence are SEQ ID NOs: 83-91. Particularly preferred examples for a peptide linker P linking two components A of the present invention are selected from the group of sequences as depicted in Table 2 below:

TABLE 2 Possible Peptide linkers SEQ ID Name: Length NO: Sequence (G)₁  1 39 G (G)2  2 40 GG (G)3  3 41 GGG (G)4  4 42 GGGG (G)5  5 43 GGGGG (G)6  6 44 GGGGGG (G)₇  7 45 GGGGGGG (G)₈  8 46 GGGGGGGG GGGS  4 47 GGGS (GGGS)₂  8 48 GGGSGGGS (GGGS)₃ 12 49 GGGSGGGSGGGS GGGGS  5 50 GGGGS (GGGGS)₂ 10 51 GGGGSGGGGS (GGGGS)₃ 15 52 GGGGSGGGGSGGGGS (SGG)₁  3 53 SGG (GSG)₁  3 54 GSG (GGS)₁  3 55 GGS (SGGG)₁  4 56 SGGG (GSGG)₁  4 57 GSGG (GGSG)₁  4 58 GGSG (SGGGG)₁  5 59 SGGGG (GSGGG)₁  5 60 GSGGG (GGSGG)₁  5 61 GGSGG (GGGSG)₁  5 62 GGGSG (SGG)₂  6 63 SGGSGG (GSG)₂  6 64 GSGGSG (GGS)₂  6 65 GGSGGS (SGGG)₂  8 66 SGGGSGGG (GSGG)₂  8 67 GSGGGSGG (GGSG)₂  8 68 GGSGGGSG (SGGGG)₂ 10 69 SGGGGSGGGG (GSGGG)₂ 10 70 GSGGGGSGGG (GGSGG)₂ 10 71 GGSGGGGSGG (GGGSG)₂ 10 72 GGGSGGGGSG (SGG)₃  9 73 SGGSGGSGG (GSG)₃  9 74 GSGGSGGSG (GGS)₃  9 75 GGSGGSGGS (SGGG)₃ 12 76 SGGGSGGGSGGG (GSGG)₃ 12 77 GSGGGSGGGSGG (GGSG)₃ 12 78 GGSGGGSGGGSG (SGGGG)₃ 15 79 SGGGGSGGGGSGGGG (GSGGG)₃ 15 80 GSGGGGSGGGGSGGG (GGSGG)₃ 15 81 GGSGGGGSGGGGSGG (GGGSG)₃ 15 82 GGGSGGGGSGGGGSG N-Glyco  9 83 GNGTSNGTS N-Glyco (1)  9 84 GNGTSNGTG N-Glyco (2)  9 85 GNGTSNGTSG N-Glyco (3)  9 86 GNGTSNGTGS N-Glyco (4) 13 87 GNGTSNGTSNGTS N-Glyco (5) 13 88 GGGSGNGTSNGTGS N-Glyco (6) 13 89 GNGTSNGTGSGGGS N-Glyco (7) 13 90 GGGSGNGTSNGTSG N-Glyco (8) 13 91 GNGTSNGTSGGGGS

A person skilled in the art will understand that the above mentioned linker peptides may also be combined and a multitude of other flexible linker sequences may be utilized in similar manner as long as they do preferably not interfere with the trimeric assembly of component A. SEQ ID NO: 48, 88 and 90 are particularly preferred as peptide linker P linking two components A of the polypeptide according to the present invention. Preferably the peptide linkers P linking the components A within the polypeptide of the present invention do not comprise any cysteine residues in order to avoid formation of intramolecular disulfide bridges which could negatively impact the trimer formation of the components A.

The at least two peptide linkers P linking the least three components A of the polypeptides according to the present invention may be in principle selected independently of each other; e.g. the at least two peptide linkers P may have the same sequence or may have different sequences (in terms of length and/or sequence). However, it is particularly preferred if the peptide linkers P linking the at least three components A are identical. Certainly, similar considerations apply if the polypeptide according to the present invention comprises more than 3 components A and more than two peptide linkers P linking said components A. The peptide linkers P are linked to the components A via a covalent bond to the C-terminus of a first component A and a covalent bond to the N-terminus of the subsequent component A. Preferably, the linkages are peptide bonds.

Specific examples of polypeptides according to the present invention comprise as components A SEQ ID NO: 5 and preferably SEQ ID NOs: 48, 88 and/or 90 as peptide linkers P.

As mentioned above, the polypeptides according to the present invention comprise alongside the at least three components A at least one component B consisting of a V_(L) region and a V_(H) region linked directly to each other with a linker sequence L which has a length of ≦12 amino acids.

The terms “V_(L)” and “V_(H)” refer to the V_(L) and V_(H) regions of an antibody, i.e. the N-terminal variable region of the light chain of an immunoglobulin and the N-terminal variable region of the heavy chain of an immunoglobulin, respectively. Both terms are well understood in the art and are structurally well defined. The individual V_(L) and V_(H) regions are each composed of 3 hypervariable regions (CDR1, CDR2, CDR3; CDR: complementarity determining region) and 4 framework regions (FR1, FR2, FR3, FR4). Identifying the respective subregions within a given sequence is routine in the art and may for example be accomplished by IgBlast of the NCBI (www.ncbi.nlm.nih.gov/igblast/), v-base of the MRC (http://vbase.mrc-cpe.cam.ac.uk/), v-base2 hosted by EU-GENE (www.vbase2.org/), on-line programs provided by the group of Andrew Martin (www.bioinf.org.uk/servers/) and/or the ExPASy Proteomics Server (http://expasy.org/). Kabat nomenclature may also be useful (http://www.bioinf.org.uk/abs/kabatman.html) (Martin, A. C. R. PROTEINS: Structure, Function and Genetics, 25 (1996), 130-133). The variable regions of the heavy and the light chain form together the binding region of an antibody. In immunoglobulins, the V_(L) and V_(H) regions are on different polypeptide chains. In the polypeptides of the present invention the V_(L) and V_(H) regions are on the same chain. Interaction of a V_(L) domain with a V_(H) domain (intra- or intermolecularly) allows the polypeptide of the present invention to bind to the respective target antigen.

Preferably, the V_(L) and the V_(H) region of the polypeptide according to the present invention are V_(L) and V_(H) regions of an antibody binding (preferably) specifically to a cell surface molecule (cell surface antigen), in particular to a cell surface molecule selected from the group consisting of: a cytokine receptor, a growth factor receptor, an integrin, a cell adhesion molecule and/or a cell type- or tissue-specific cell surface antigen, cell surface expressed tumor-associated antigens (TAA), carbohydrates. A tumor-associated antigen may for example be expressed on tumor cells per se, on malignant cells, on stroma cells, on tumor endothelium and other tumor localized cell types.

In a preferred embodiment the V_(L) and the V_(H) region of the polypeptide according to the present invention are V_(L) and V_(H) regions of an antibody binding to a target antigen selected from the group consisting of: the erbB family of tyrosine kinase receptors (EGFR, HER2, HER3, HER4), VEGFRs, hetermeric integrin a_(x) β_(x) receptor family, fibroblast activation protein (FAP), galectin, EpCAM, CEA, CD44 and tumor specific variants thereof (CD44v) and other tumor selective cell surface markers, CD2, CD5, CD7, CD19, CD20, CD21, CD22, CD24, CD25, CD30, CD33, CD38, CD40, CD52, CD56, CD71, CD72, CD73, CD105, CD117, CD123, c-Met, PDGFR, IGF1-R, HMW-MAA, TAG-72, GD2, GD3, GM2, folate receptor, Le^(y), MUC-1, MUC-2, PSMA, PSCA, uPAR, Claudin 18.2, etc. Particularly preferred targets are the members of the erbB family of tyrosine kinase receptors and tumor stroma selective targets such as FAP.

As proof of concept, EGFR is used as target antigen in the appended examples.

Respective V_(H) and V_(L) sequences may easily be obtained by a person skilled in the art. Polypeptide and nucleic acid sequences for many antibodies are readily available in the art (see for example Expasy sequence database, PubMed etc.). Alternatively, a person skilled in the art may determine the sequence of available antibodies of the desired specificity or may even produce a new antibody against the desired target antigen by immunizing an animal suitable for antibody production with the antigen, isolating antigen specific B-cell clones and sequencing the respective V_(L) and V_(H) genes. Antibodies (and subsequently antibody sequences) may also be obtained from recombinant antibody libraries, e.g. immune, naive, semi-synthetic or fully synthetic antibody libraries. Isolation from such libraries can be achieved by different means, e.g. by phage display, ribosome display, yeast display, bacterial display, high-throughput screening, etc. By means of genetic engineering said sequences may then be included in a nucleic acid sequence encoding a polypeptide of the present invention.

A person skilled in the art will understand that the V_(H) and V_(L) regions in the polypeptide according to the present invention may be artificial, i.e. need not be derived from a de facto naturally occurring antibody. Rather this terminology is intended to reflect that said regions exhibit the general architecture of V_(L) and V_(H) regions. The V_(L) and V_(H) regions of the polypeptides according to the present invention may for example be humanized sequences, e.g. while the CDRs are of mouse origin, the framework regions are of human origin. The V_(L) and V_(H) regions may be for example deimmunized and/or fully human.

A particularly preferred V_(L) region is SEQ ID NO: 92 if the target antigen is EGFR (see for example in SEQ ID NOs: 102 and 107).

A particularly preferred V_(H) region is SEQ ID NO: 93 if the target antigen is EGFR (see for example in SEQ ID NOs: 102 and 107).

Particularly preferred V_(L) regions if the target antigen is FAP are the amino acid sequences according to SEQ ID NOs: 130-132 (see for example in SEQ ID NOs: 127-129).

Particularly preferred V_(H) regions if the target antigen is FAP are the amino acid sequences according to SEQ ID NOs: 133-135 (see for example in SEQ ID NOs: 127-129).

The TRAIL fusion proteins according to SEQ ID NOs: 127-129 are examples of tumorstroma targeted TRAIL fusion proteins recognizing the selective tumorstroma marker fibroblast activation protein (FAP). Thus, TRAIL proapoptotic activity is directed to the tumor environment and through juxtatropic presentation of the TRAIL module within the fusion protein, apoptosis is signaled in trans to the tumor cell. Highly specific apoptotic activity of the TRAIL module ensures efficient antitumoral therapeutic action towards a wide variety of carcinomas, as FAP overexpression is a prominent and common feature of a variety of epithelial cancers, including breast, colon, pancreas and lung, with a variable stroma content comprising 10 to 90% of total tumor mass (Garin Chesa et al, 1990, PNAS 87:7235-7239).

The fusion proteins according to SEQ ID NOs: 127-129 are FAP specific and exhibit high binding affinity typically in the nanomolar range (e.g. 10-30 nM). The components B of the fusion proteins according to SEQ ID NOs: 127-129 are 1) a humanized variant, generated by CDR grafting, and being species crossreactive between mouse and human (SEQ ID NOs: 130, 133, 136 and 127), thus allowing preclinical studies in murine tumor models; 2) two fully human components B, isolated by guided selection from a naïve human Ig library (SEQ ID NOs: 131, 134, 137 and 128, and SEQ ID NOs: 132, 135, 138 and 129) and binding to different epitopes at the extracellular domain of human FAP, one characterized by competition with the murine mab F19 (SEQ ID NOs: 131, 134, 137 and 128), the other one not competing with F19 for FAP binding (SEQ ID NOs: 132, 135, 138 and 129).

The V_(L) region and the V_(H) region may be arranged in any suitable manner in the polypeptide according to the present invention. Preferably, the region comprising the V_(L) region and the V_(H) region is arranged N-terminally of the region comprising the three components A.

As mentioned above, the V_(L) region and a V_(H) region of component B of the polypeptides according to the present invention are linked directly to each other with a linker sequence L which has a length of ≦12 amino acids. Linker sequence L is preferably a flexible amino acid stretch. Preferably, such linker sequence L is less than 11, even more preferably less than 10, even more preferably less than 9, even more preferably less than 8, even more preferably less than 7, even more preferably less than 6 amino acids long. In addition, the linker sequence L may have preferably an amino acid length of 0 amino acids or more, 1 amino acid or more, 2 amino acids or more, 3 amino acids or more, 4 amino acids or more, 5 amino acids or more, 6 amino acids or more, 7 amino acids or more, and/or 8 amino acids or more. A linker sequence L linking the V_(L) and V_(H) region of a component B of a polypeptide of the present invention may thus have for example an amino acid length in the range of 0 to 12 amino acids, 1 to 12 amino acids, 2 to 10 amino acids, 3 to 10 amino acids, 3 to 9 amino acids, 3 to 6 amino acids, 4 to 8 amino acids, 4 to 7 amino acids, 4 to 12 amino acids or any other combination of amino acids lengths disclosed above for linker sequence L. Particularly preferred are linker sequence L lengths of 0 to 5 amino acids, in particular 5 amino acids.

In terms of amino acid sequence, the linker sequence L linking the V_(L) and V_(H) region of a component B of a polypeptide of the present invention is preferably a glycine (G) rich peptide linker, i.e. has an amino acid sequences with a high glycine content of more than 50%; e.g. from at least 60 to 90%, for example of about 80%. Other amino acids which may be present in the linker sequence L are for example serine residues or less preferably alanine residues or glutamine residues. The linker sequence L may be composed of repetitive units. For example the linker may comprise two, three or four units of GG (SEQ ID NO: 40); GGS (SEQ ID NO: 55); GSG (SEQ ID NO: 54), or SGG (SEQ ID NO: 53) and combinations thereof. Particularly preferred examples for a linker sequence L linking the V_(L) and V_(H) region of a component B of a polypeptide of the present invention are selected from the group of sequences as depicted in Table 2 above (except for those sequences exceeding the length restriction of linker sequence L. Thus, if a linker sequence L is present, the linker sequence L may for example be selected from linker sequences of SEQ ID NOs. 39-51, and 53-78.

SEQ ID NO: 50 is particularly preferred as linker sequence L linking the V_(L) and V_(H) region of a component B of a polypeptide of the present invention. Preferably the linker sequence L does not comprise any cysteine residues in order to avoid formation of intramolecular disulfide bridges, which could for example negatively impact the correct formation of the V_(H) or V₁ secondary structure of the polypeptide according to the present invention.

Linker sequence L may certainly be selected independently for each component B present in the polypeptide according to the present invention and independently of any peptide linker P selected for linking the components A. Linker sequence L links the V_(L) region and the V_(H) region via a covalent bond. Preferably the linkages are peptide bonds. Component B may have (from N- to C-Terminus) the sequence:

-   -   V_(L) region-linker sequence L-V_(H) region         or may have the sequence     -   V_(H) region-linker sequence L-V_(L) region.

The arrangement V_(H) region-linker sequence L-V_(L) region is particularly preferred.

In a particularly preferred embodiment, component B has the sequence of SEQ ID NO: 94 which is composed of SEQ ID NOs: 93, 50 and 92 (see for example in SEQ ID NOs: 102 and 107).

In this context the present invention also relates to a polypeptide comprising the sequence of SEQ ID NO: 92, SEQ ID NO: 93, SEQ ID NO: 92 and SEQ ID NO: 93, and/or SEQ ID NO: 94.

In further particularly preferred embodiments, component B has the sequence of any of SEQ ID NOs: 136-138 which are composed of SEQ ID NOs: 133, 50 and 130 (see for example in SEQ ID NO: 127), SEQ ID NOs: 134, 50 and 131 (see for example in SEQ ID NO: 128), and SEQ ID NOs: 135, 50 and 132 (see for example in SEQ ID NO: 129), respectively.

In this context the present invention also relates to a polypeptide comprising the sequence according to SEQ ID NO: 130, SEQ ID NO: 133, SEQ ID NO: 130 and SEQ ID NO: 133, and/or SEQ ID NO: 136, to a polypeptide comprising the sequence according to SEQ ID NO: 131, SEQ ID NO: 134, SEQ ID NO: 131 and SEQ ID NO: 134, and/or SEQ ID NO: 137, and to a polypeptide comprising the sequence according to SEQ ID NO: 132, SEQ ID NO: 135, SEQ ID NO: 132 and SEQ ID NO: 135, and/or SEQ ID NO: 138.

It will be understood by a person skilled in the art that a component B of a polypeptide according to the present invention does not comprise any antibody constant regions such as in Fab fragments.

Polypeptides according to the present invention comprise at least three components A and at least one component B. Preferably, the region comprising the at least three components A is linked to component B via a peptide linker X. Peptide linker X can in principle be any sequence as long as it does neither interfere with formation of the THD trimer nor with the association of a V_(H) domain with a V_(L) domain. In particular, there is no absolute length restriction with regard to linker X and no requirement for flexibility. However, preferably X is less than 50, even more preferably less than 45, even more preferably less than 40, even more preferably less than 35, even more preferably less than 30, even more preferably less than 25, even more preferably less than 20, even more preferably ≦15 amino acids long. Thus, linker X can be for example a linker as defined above for peptide linkers P or linking sequence L. In a particularly preferred embodiment linker X may for example comprise the sequence GNGTSNGTS (SEQ ID NO:83), which allows for glycosylation of a polypeptide of the present invention and thus improves stability of the overall polypeptide. The glycosylation residues are then the Asn residues. Specific examples for sequences of linker X may for example be AAAEFTRG (SEQ ID NO: 95), AAAGNGTSNGTSEFTRG (SEQ ID NO: 105), and GGSGNGTSNGTSG (SEQ ID NO: 106). The latter two allow again for glycosylation of the polypeptide according to the present invention.

The structure of the polypeptide according to the present invention may for example comprise (from N- to C-Terminus; B: component B; X: peptide linker X; A: a component A; P: peptide linker P):

-   -   B-X-A-P-A-P-A,         or may be     -   A-P-A-P-A-X-B.

Specific examples of polypeptides according to the present invention comprise as components A SEQ ID NO: 5 and as component B SEQ ID NO: 94, preferably with SEQ ID NOs: 48, 88 and/or 90 as peptide linkers P. SEQ ID NO: 102 and SEQ ID NO: 107 (SEQ ID NO: 107 corresponds to amino acids 34-850 of SEQ ID NO: 102, i.e. does not include the leader sequence and the FLAG tag) are preferred examples of the present invention. Further preferred examples of the polypeptides according to the present invention, are sequences according to SEQ ID NOs: 125 and 126 comprising an albumin binding domain (ABD), and sequences according to SEQ ID NOs: 127-129 comprising a FAP-specific component B.

In a further aspect, the present invention relates to a polypeptide which comprises the sequence of SEQ ID NO: 96.

In a further aspect the present invention relates to a polypeptide which comprises:

-   -   a) at least three components A, each of which comprises the         sequence of a TNF homology domain (THD) of a TNF ligand family         member, or functional derivative thereof, and     -   b) a sequence comprising a glycosylation motif.

Glycosylation motifs comprise for instance nitrogen atoms in asparagine or arginine side-chains. Examples for glycosylation motifs are disclosed for instance above in SEQ ID NOs: 83-91. Specific examples of such polypeptides are polypeptides comprising the sequence of SEQ ID NO: 97, or SEQ ID NO: 98.

Besides, the polypeptides according to the present invention should preferably not comprise any endopeptidase recognition and/or cleavage sites, at least not within the structures B-X-A-P-A-P-A or A-P-A-P-A-X-B, respectively (presence of endopeptidase cleavage sites N- or C-terminal thereof will not affect the overall function of the polypeptide according to the present invention and their presence is thus not critical). In other words, the polypeptide according to the present invention should preferably not comprise any endopeptidase recognition and/or cleavage sites within the region comprising the at least three components A and the at least one component B and the linker in between. Presence of endopeptidease cleavage sites will significantly reduce the half-life of a polypeptide according to the present invention and may severely impact the efficacy of the polypeptide according to the present invention, because interaction of important domains is abolished. For example, separation of one component A from the polypeptide according to the present invention via endopeptidase cleavage will prevent trimer formation. Likewise, if component B is separated from the components A, any targeting effect is lost. This may be prevented by removing/altering respective endopeptidase recognition sites, by removing the endopeptidase cleavage sites and or by doing both. In this context, it is particularly preferred, if the components A in the polypeptide according to the present invention do not comprise a TACE cleavage site. TACE (TNF-alpha-converting enzyme, also termed ADAM17) is a member of the ADAM protease family and represents the enzyme physiologically processing for example the initially membrane bound TNF and others. TACE cleaves the membrane bound form whereby TNF is released (shed). Thus, a TNF based component A preferably lacks the Ala76-Val77 cleavage site of TNF. Lacking the cleavage site implies that the cleavage site may be deleted or is altered e.g. by means of substitution or insertion. Alternatively, or preferably in addition, the protease binding site within the stalk region of a TNF ligand, e.g. amino acid 77-88 of TNF-(Val-Arg-Ser-Ser-Ser-Arg-Thr-Pro-Ser-Glu-Lys-Pro), may be altered (or preferably deleted) to avoid recognition of the polypeptide of the present invention by TACE.

Polypeptides according to the present invention may comprise further polypeptide sequences and domains, which are however entirely optional.

One such optional element which may or may not be present in a polypeptide according to the present invention is the presence of one or more albumin binding domains (ABDs) within a polypeptide according to the present invention. The polypeptides according to the present invention may further comprise such an albumin binding domain in particular with the purpose to prolong the plasma half-life of the polypeptide of the present invention and thereby maintain therapeutically effective plasma concentrations. Serum albumin possesses an extraordinary long plasma half-life in humans. The plasma half-life of human serum albumin is in the range of 19 days. Apart from IgG no other soluble serum protein is known to exhibit such long half-life. The albumin binding domain (ABD) may be any molecule with affinity for albumin such as certain peptides, antibody fragments, alternative scaffolds, and small chemicals (for review see Kontermann BioDrugs 2009, 23:93-109, incorporated herein by reference). Particularly preferred examples of albumin binding domains in a polypeptide according to the present invention are selected for example from the group consisting of: albumin binding antibodies and albumin binding antibody derivatives, such as albumin binding Fab fragments, albumin binding scFv antibodies, and protein G of Streptococcus strain G148. Most preferred is the ABD of protein G of Streptococcus strain G148 comprising the sequence QHDEAVDANSLAEAKVLANRE LDKYGVSDYYKNLINNAKTVEGVKALIDEILAALP (SEQ ID NO: 99) and non-immunogenic variants or derivatives thereof (e.g. as described in Johnsson et al. Protein Eng. Des. Sel. 21 (2008) pp 515-527 and Hopp et al. Protein Eng. Des. Sel. 23 (2010) pp 827-834, both incorporated herein by reference). Alternatively, the polypeptide according to the present invention may simply be a fusion protein with albumin moiety itself, or a fragment or derivative thereof. An example of such polypeptide is SEQ ID NO: 103.

In a particularly preferred embodiment, the polypeptide according to the present invention comprises an albumin binding domain as described above, for example an albumin binding domain according to SEQ ID NO: 99 or a derivative thereof which is capable of binding albumin, such as a sequence having at least 60% identity, preferably at least 70% identity, more preferably at least 80%, even more preferably at least 90% identity to SEQ ID NO: 99 over the entire length of SEQ ID NO: 99, or a fragment of SEQ ID NO: 99 or of a derivative thereof capable of binding albumin, such as a fragment consisting of a continuous stretch of amino acids representing at least 40%, preferably at least 50%, preferably at least 60%, more preferably at least 70%, even more preferably at least 80% of the full length sequence of SEQ ID NO: 99 or of a derivative thereof.

Preferably, the position of the ABD within the polypeptide according to the present invention is selected such that it does not significantly interfere with the bioactivity of the polypeptide according to the present invention, e.g. of inducing apoptosis in target cells, such as cancer cells. It is particularly preferred that the optional ABD is located between components A and component B of the polypeptide according to the present invention. For example, in a particularly preferred embodiment, component B is located N-terminally to components A and the optional ABD is located between components A and component B, e.g. forming a fusion protein having the structure N-K-[component B]-X-ABD-P-[components A]-X-C, wherein K is an optional V_(H) leader sequence, X and P are optional linkers as described herein which may or may not comprise a glycosylation site, and N and C represent the N-terminal and the C-terminal end of the fusion protein, respectively. An example for such a polypeptide according to the present invention is given in SEQ ID NO: 125 (FIG. 25).

In another particularly preferred embodiment, the optional albumin binding domain is located downstream of components A of the polypeptide according to the present invention. For example, in a particularly preferred embodiment, component B is located N-terminally to components A and the optional ABD is located C-terminally to components A. Thus, in a particularly preferred embodiment, the polypeptide according to the present invention exhibits the structure N-K-[component B]-X-[components A]-P-ABD-X-C, wherein K is an optional V_(H) leader sequence, X and P are optional linkers as described herein which may or may not comprise a glycosylation site, and N and C represent the N-terminal and the C-terminal end of the fusion protein, respectively. Preferably, ABD is located at the C-terminal end of the polypeptide according to the present invention. An example of such a polypeptide according to the present invention is given in SEQ ID NO: 126 (FIG. 26).

Another optional element which may or may not be present in a polypeptide according to the present invention is a tag allowing for example the detection and or purification of a polypeptide according to the invention. Examples for such tags are for example a His-tag, a FLAG-tag (DYKDDDDK; SEQ ID NO: 100), a HA-tag, a STREP-tag, a myc-tag, GST. Preferably, such tag is positioned outside the region comprising the at least three components A and the at least one component B. If so, it is possible to position a protease cleavage site (such as a thrombin cleavage site) adjacent to the tag, e.g. directly C-terminally of the tag. This will allow to remove the tag for example after purification.

Another optional but preferred element which may or may not be present in a polypeptide according to the present invention is a leader or signal peptide sequence such as the V_(H) leader sequence MDWTWRVFCLLAVAPGAHS (SEQ ID NO: 101) or Igκ (METDTLLLWVLLLWVPGSTG; SEQ ID NO: 108). Such sequences may affect processing and targeting of the polypeptide according to the present invention after translation if produced in matching cell systems. For example, the V_(H) leader sequence (if used for example in a mammalian) directs a polypeptide according to the present invention into the secretory pathway and thus allows for easier purification of the secreted product from culture supernatants. As with the detection and purification tags mentioned above, such leader or signal peptide sequence is positioned at the very N-Terminus of the polypeptide according to the present invention, thus allowing a cotranslational translocation into the ER and physiological processing in suitable mammalian expression systems such as CHO cells. In this regard a person skilled in the art will understand that if herein a polypeptide sequence is given with a leader sequence herein, then said polypeptide will for example after expression in a mammalian expression no longer comprise said leader sequence. Certainly, any such polypeptide without leader sequence falls within the scope of the present invention. In particular, polypeptides comprising the sequence of SEQ ID NOs: 96, 97, 98, 102, and/or 103 without the leader sequence of SEQ ID NO: 101 are embodiments of the present invention. Likewise, polypeptides comprising the sequence of SEQ ID NOs: 96, 97, 98, 102, and/or 103 without the leader sequence of SEQ ID NO: 101 and without the FLAG tag sequence of SEQ ID NO: 100 are embodiments of the present invention.

Likewise a polypeptide according to the present invention may optionally exhibit modifications. For instance, the polypeptide according to the present invention may be altered with regard to its hydrodynamic volume. The hydrodynamic volume of a protein can be increased by attaching highly flexible, hydrophilic molecules such as polyethylene glycol and/or carbohydrates. PEGylation, i.e. the chemical coupling of polyethylene glycol (PEG) is frequently used in the art. PEG is composed of ethylene oxide units connected in a linear or branched configuration and of varying length. For example, one or several PEG chains of 5 to 40 kDa may be conjugated to a polypeptide according to the present invention. However, PEGylation should preferably not be achieved in random manner because such approach may negatively impact the trimerization or targeting properties of the polypeptides according to the present invention. Preferably, the PEGylation sites are not within the region comprising the at least three components A and the at least one component B. PEG moieties may for example be attached to the polypeptide according to the present invention via cysteine residues. These cysteine residues are preferably positioned outside the region comprising the at least three components A and the at least one component B.

Several other techniques are also known in the art. PEG mimetics may certainly also be used to modify the polypeptides according to the present invention.

A further possible modification of the polypeptides according to the present invention is—as already indicated above—glycosylation. Glycosylation can positively influence the half-life and stability of a polypeptide according to the present invention. N- as well as O-glycosylation may be contemplated. The inventors of the present invention have for example shown that glycosylation is possible by introducing a linker X which has the sequence GNGTSNGTS (SEQ ID NO: 83). Glycosylation sites at other sequence positions of the polypeptide according to the present invention are certainly also possible. Preferably, such glycosylation sites do not (significantly) impact the targeting and the respective functional activity of the THD of the TNF ligand family member within the polypeptide according to the present invention. Examples for such polypeptides are the polypeptides with the sequence of SEQ ID NO: 97, 98 and 103.

Other possible modifications of the polypeptides according to the present invention include for example HESylation (modification with hydroxyethyl starch) and modification with polysialic acid (PSA).

In general, the production of polypeptides is well-known in the art and a person skilled in the art can easily arrive at a polypeptide according of the present invention by means of routine methods (see for example Maniatis, et al. (2001), Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press). In general, the production of polypeptides and proteins, respectively, is achieved by creating a DNA sequence encoding the same, followed by subsequent transformation of a suitable host with the respective DNA sequence and expression of the modified DNA sequence. Alternatively, the polypeptides according to the present invention may be chemically synthesized.

The present invention relates also to polypeptide complexes of the polypeptides according to the present invention, e.g. homodimeric and/or homotrimeric complexes of polypeptides according to the present invention. Thus, the polypeptide according to the present invention is preferably capable of forming multimers, such as dimers, trimers, tetramers etc., preferably dimers. Preferably, component B is capable of forming multimers, such as dimers, trimers, tetramers etc. Thus, in a particular preferred embodiment, component B is selected such that multimerization, such as dimerization, of the polypeptide according to the present invention is possible. In a particularly preferred embodiment, the polypeptide according to the present invention exhibits a multimeric form, such as a dimeric, trimeric, tetrameric etc. form, most preferably a dimeric form. Thus, preferably the polypeptide according to the present invention is multimeric, such as dimeric, trimeric or tetrameric, preferably dimeric. Accordingly, in a particular preferred embodiment the polypeptide complex according to the present invention is dimeric. A dimeric polypeptide according to the present invention comprises at least 6 components A.

In a further aspect the present invention also relates to a nucleic acid encoding a polypeptide according to the present invention. The nucleic acid may be DNA or RNA or a hybrid thereof. Preferably, the nucleic acid also comprises sequences allowing for the expression of the polypeptide according to the present invention in a suitable expression system. The nucleic acid can be codon optimized for the respective expression system.

In a further aspect the present invention also relates to a vector comprising a nucleic acid according to the present invention. Preferably, the vector provides for transcription and expression of the polypeptide according to the present invention in a suitable host cell system.

In a further aspect the present invention also relates to a (host) cell comprising a nucleic acid according to the present invention, a vector according to the present invention, a polypeptide according to the present invention, or a polypeptide complex according to the present invention. If the host cell is a human host cell, it is an isolated host cell outside the human body.

In a further aspect the present invention relates to a non-human organism comprising a nucleic acid according to the present invention, a vector according to the present invention, a polypeptide according to the present invention, a polypeptide complex according to the present invention or a host cell according to the present invention.

In a further aspect the present invention relates to nucleic acid according to the present invention, a vector according to the present invention, a polypeptide according to the present invention, a polypeptide complex according to the present invention and/or a host cell according to the present invention in a method for treatment of the human or animal body by surgery or therapy and diagnostic methods practised on the human or animal body. Preferably, the method of treatment relates to the treatment of cancer, autoimmune or degenerative diseases.

In this context the present invention also relates to a pharmaceutical composition comprising a nucleic acid according to the present invention, a vector according to the present invention, a polypeptide according to the present invention, a polypeptide complex according to the present invention and/or a host cell according to the present invention and optionally a pharmaceutically acceptable carrier, adjuvant, and/or vehicle. A particularly preferred pharmaceutical composition comprises a polypeptide comprising the sequence of SEQ ID NO: 102, 103, 107, 125, 126, 127, 128 and/or 129.

The pharmaceutical composition typically comprises a safe and effective amount of the compounds according to the invention (polypeptides, nucleic acids, vectors) as defined above.

As used here, “safe and effective amount” means an amount of the compounds as defined above, that is sufficient to significantly induce a positive modification of a condition to be treated, for example of cancer and/or a tumor. At the same time, however, a “safe and effective amount” is preferably small enough to avoid serious side-effects, that is to say to permit a sensible relationship between advantage and risk. The determination of these limits typically lies within the scope of sensible medical judgment. A “safe and effective amount” of the compounds according to the invention as defined above will vary in connection with the particular condition to be treated and also with the age and physical condition of the patient to be treated, the severity of the condition, the duration of the treatment, the nature of the accompanying therapy, of the particular pharmaceutically acceptable carrier used, and similar factors, within the knowledge and experience of the accompanying doctor. The medicament according to the invention can be used according to the invention for human and also for veterinary medical purposes, as a pharmaceutical composition.

The pharmaceutical composition of the present invention typically contains a pharmaceutically acceptable carrier. The expression “pharmaceutically acceptable carrier” as used herein preferably includes the liquid or non-liquid basis of the inventive medicament. If the inventive medicament is provided in liquid form, the carrier will typically be pyrogen-free water; isotonic saline or buffered (aqueous) solutions, e.g. phosphate, citrate etc. buffered solutions. Particularly for injection of the inventive medicament, a buffer, preferably an aqueous buffer, may be used, containing a sodium salt. The injection buffer may be hypertonic, isotonic or hypotonic with reference to the specific reference medium, i.e. the buffer may have a higher, identical or lower salt content with reference to the specific reference medium, wherein preferably such concentrations of the afore mentioned salts may be used, which do not lead to damage of cells due to osmosis or other concentration effects. Reference media are e.g. in “in vivo” methods occurring liquids such as blood, lymph, cytosolic liquids, or other body liquids, or e.g. liquids, which may be used as reference media in “in vitro” methods, such as common buffers or liquids. Such common buffers or liquids are known to a skilled person. Ringer-Lactate solution is particularly preferred as a liquid basis.

However, one or more compatible solid or liquid fillers or diluents or encapsulating compounds may be used as well, which are suitable for administration to a person. The term “compatible” as used here means that the constituents of the inventive medicament are capable of being mixed with the compound according to the invention as defined above in such a manner that no interaction occurs which would substantially reduce the pharmaceutical effectiveness of the inventive medicament under usual use conditions. Pharmaceutically acceptable carriers must, of course, have sufficiently high purity and sufficiently low toxicity to make them suitable for administration to a person to be treated. Some examples of compounds which can be used as pharmaceutically acceptable carriers or constituents thereof are sugars, such as, for example, lactose, glucose and sucrose; starches, such as, for example, corn starch or potato starch; cellulose and its derivatives, such as, for example, sodium carboxymethylcellulose, ethylcellulose, cellulose acetate; powdered tragacanth; malt; gelatin; tallow; solid glidants, such as, for example, stearic acid, magnesium stearate; calcium sulfate; vegetable oils, such as, for example, groundnut oil, cottonseed oil, sesame oil, olive oil, corn oil and oil from theobroma; polyols, such as, for example, polypropylene glycol, glycerol, sorbitol, mannitol and polyethylene glycol; alginic acid.

The choice of a pharmaceutically acceptable carrier is determined in principle by the manner in which the inventive medicaments are administered. The inventive medicaments can be administered, for example, systemically. Routes for administration include, for example, transdermale, inhalation, oral, parenteral, including subcutaneous or intravenous injections, topical and/or intranasal routes. The suitable amount of the inventive medicament to be administered can be determined by routine experiments with animal models. Such models include, without implying any limitation, rabbit, sheep, mouse, rat, dog and non-human primate models. Preferred unit dose forms for injection include sterile solutions of water, physiological saline or mixtures thereof. The pH of such solutions should be adjusted to about 7.4. Suitable carriers for injection include hydrogels, devices for controlled or delayed release, polylactic acid and collagen matrices. Suitable pharmaceutically acceptable carriers for topical application include those which are suitable for use in lotions, creams, gels and the like. If the inventive medicament is to be administered perorally, tablets, capsules and the like are the preferred unit dose form. The pharmaceutically acceptable carriers for the preparation of unit dose forms which can be used for oral administration are well known in the prior art. The choice thereof will depend on secondary considerations such as taste, costs and storability, which are not critical for the purposes of the present invention, and can be made without difficulty by a person skilled in the art.

All references cited herein are incorporated herein in their entirety.

In the following a brief description of the appended figures will be given. The figures are intended to illustrate the present invention in more detail. However, they are not intended to limit the subject matter of the invention to any extent.

FIG. 1: Schematic illustration of exemplary polypeptides according to the present invention:

A) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, e.g. 15 aa long (e.g. (GGGGS)₃; SEQ ID NO:         52);     -   X=peptide linker X (see for instance SEQ ID NO: 95);     -   P=peptide linker P (e.g. SEQ ID NO: 48);     -   A=component A (e.g. TRAIL aa residues 95-281, SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 96 (FIG. 20).

B) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, ≦12 aa long (e.g. (GGGGS); SEQ ID NO:50);     -   X=peptide linker X (see for instance SEQ ID NO: 95);     -   P=peptide linker P (e.g. SEQ ID NO: 48);     -   A=component A (e.g. TRAIL aa residues 95-281; SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 102 (FIG. 21).

C) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, e.g. 15 aa long (e.g. (GGGGS)₃; SEQ ID NO:         52);     -   X=peptide linker X including glycosylation site (see for         instance SEQ ID NO: 105);     -   P=peptide linker P (e.g. SEQ ID NO: 48);     -   A=component A (e.g. TRAIL aa residues 95-281; SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 97 (FIG. 22).

D) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, e.g. 15 aa long (e.g. (GGGGS)₃; SEQ ID NO:         52);     -   X=peptide linker X including glycosylation site (see for         instance SEQ ID NO: 105);     -   P=peptide linker P including glycosylation site (e.g. P₁: (SEQ         ID NO: 90); P₂: SEQ ID NO: 88);     -   A=component A (e.g. TRAIL aa residues 95-281; SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 98 (FIG. 23).

E) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   ABD=Albumin binding domain (see for instance SEQ ID NO: 99);     -   Q=Linker sequence (e.g. GGSGGGGSGG; SEQ ID NO: 71);     -   L=linker sequence L, ≦12 aa long (e.g. (GGGGS); SEQ ID NO: 50);     -   X=peptide linker X including glycosylation site (see for         instance SEQ ID NO: 106);     -   P=peptide linker P with (e.g. SEQ ID NO: 88) or without         glycosylation site (e.g. SEQ ID NO 48: GGGSGGGS);     -   A=component A (e.g. TRAIL aa residues 95-281, SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 103 (FIG. 24).

F) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, ≦12 aa long (e.g. (GGGGS); SEQ ID NO: 50);     -   Q=Linker sequence (e.g. GGS; SEQ ID NO: 55);     -   ABD=Albumin binding domain (see for instance SEQ ID NO: 99);     -   X=peptide linker X including glycosylation site (see for         instance SEQ ID NO: 105);     -   P=peptide linker P (e.g. GGGSGGGS; SEQ ID NO: 48);     -   A=component A (e.g. TRAIL aa residues 95-281, SEQ ID NO: 5).     -   An example for such polypeptide is SEQ ID NO: 125 (FIG. 25).

G) K=V_(H) leader (e.g. SEQ ID NO: 101);

-   -   F=tag (i.e. FLAG tag; see for instance SEQ ID NO: 100);     -   L=linker sequence L, ≦12 aa long (e.g. (GGGGS); SEQ ID NO: 50);     -   X=peptide linker X including glycosylation site (see for         instance SEQ ID NO: 105);     -   P₁=peptide linker P₁ (e.g. GGGSGGGS; SEQ ID NO: 48);     -   P₂=peptide linker P₂ (e.g. GGSGG; SEQ ID NO: 61);     -   A=component A (e.g. TRAIL aa residues 95-281, SEQ ID NO: 5);     -   ABD=Albumin binding domain (see for instance SEQ ID NO: 99).     -   An example for such polypeptide is SEQ ID NO: 126 (FIG. 26).

FIG. 2: Purified polypeptides of SEQ ID NO: 104 (lane 1), SEQ ID NO: 96 (lane 2), SEQ ID NO: 102 (lane 3) and of glycosylated SEQ ID NO: 97 (lane 4) were analyzed by SDS-PAGE (reducing conditions) followed by silver staining (upper, left, 1 μg protein per lane) or Western blotting (lower, 250 ng protein per lane) using monoclonal anti-TRAIL or anti-FLAG antibodies in combination with alkaline phosphatase-conjugated secondary antibody. The glycosylated polypeptide of SEQ ID NO: 97 was treated with N-glycosidase and analysed by SDS-PAGE and Coomassie staining (upper, right). SEQ ID NO: 104 is a single chain TRAIL polypeptide with three copies of TRAIL 95-281 (SEQ ID NO: 5) linked by two glycine linkers and comprising an N-terminal Flag-tag. However, the polypeptide does not comprise any region B as specified herein.

FIG. 3 Purified polypeptides of SEQ ID NO: 104 (upper left), SEQ ID NO: 96 (lower left), SEQ ID NO: 102 (upper right) and of glycosylated SEQ ID NO: 97 (lower right) were separated by size exclusion chromatography on a BioSuite 250 column. The retention times of the molecular weight standards thyroglobulin (669 kDa), β-amylase (200 kDa), bovine serum albumin (67 kDa) and carbonic anhydrase (29 kDa) are indicated by dotted lines.

FIG. 4 Flow cytometric analysis of expression of EGF receptor and proapoptotic TRAIL receptors DR4 and DR5 in Jurkat, Huh-7 and HepG2 cell lines.

FIG. 5 Flow cytometric analysis: (A) Blocking of the binding of Cetuximab to target-negative (HepG2) and target-positive cells (Huh-7) by an excess of SEQ ID NO: 102; (B) Binding of SEQ ID NO: 102 and SEQ ID NO: 96 to HepG2 and Huh-7 cells. “scFv” represents an anti-EGFR specific antibody fragment used for competition.

FIG. 6 Target-independent induction of cell death: (A) EGFR low/negative HepG2 cells were sensitized with 500 ng/ml Bortezomib and treated with serial dilutions of SEQ ID NO: 102 (open squares), KillerTRAIL™ (inverted filled triangle), SEQ ID NO: 96 (open circles) and SEQ ID NO:104. Cell viability was determined using crystal violet staining. Results from four independent experiments are shown (mean±S.E.M.). (B) Jurkat cells (1×10⁵/well) were used for a similar experiment as described in (A). Jurkat cells were not sensitized. Results from three independent experiments are shown (mean±S.E.M.). Viability of Jurkat cells was determined using the MTT assay.

FIG. 7. EGFR-directed induction of cell death in EGFR+ Huh-7 hepatocellular carcinoma cells sensitized with 250 ng/ml Bortezomib and treated in duplicates with serial dilutions of SEQ ID NO: 102 (open squares), SEQ ID NO: 96 (open circles), SEQ ID NO: 97 (open diamond), and SEQ ID NO: 104 as control (left side of panel). For quantification of the targeting effect, cells were additionally preincubated with an excess of EGFR-specific antibody Cetuximab (70 nM) before adding the test polypeptides (graphs of SEQ ID NO: 102 (middle panel) and SEQ ID NO: 96 (right panel). For easy comparison, dose response curves of the respective reagents in absence of cetuximab from the left panel were plotted again in these two panels. Results from four independent experiments are shown (mean±S.E.M.).

FIG. 8: EGFR-directed induction of cell death in Huh-7 hepatocellular carcinoma cells as in FIG. 7 with the exception that constant concentrations of the test proteins were used for preincubation (30 min), followed by addition of serial dilutions of Bortezomib. Control: Bortezomib alone. Results from three independent experiments are shown (mean±S.E.M.).

FIG. 9: EGFR specific TRAIL fusion proteins lack hepatotoxic activity. Groups of 3 CD1 mice were treated intraperitonally with indicated fusion proteins or control reagents: negative control: PBS; positive control: aggregated FasL (CD95L) fusion protein. (A) Plasma samples were prepared after 4 h and 24 h and the activity of alanine aminotransferase (ALT) was assayed using an enzymatic assay (Bioo Scientific, Austin, Tex.). Dashed line indicates upper normal level of ALT (physiologic range in adult human: 35-50 U/L). (B) Mice were sacrificed after 24 h except for positive control (animals treated with an aggregated FasL (CD95L) fusion protein show phenotypic signs of severe systemic toxicity after 2-4 hrs and die after ˜5 hrs, samples were taken after 4 hrs) and liver biopsies were taken for determination of caspase-3 activity using a specific AMC-coupled peptide substrate (Enzo Lifesciences, Lörrach, Germany).

FIG. 10: EGFR-directed induction of cell death by single-chain TRAIL fusions on NCI-H460 cells. NCI-H460 non-small lung cancer cells (3×10⁴/well) were seeded in 96-well plates and cultivated for 24 h. Then, cells were sensitized with 2.5 μg/ml cycloheximide and treated in duplicates with serial dilutions of the indicated fusion proteins. After 16 h, cell viability was determined using crystal violet staining. Results from two independent experiments are shown (mean±S.E.M.). EC₅₀ values were 1.2±0.08×10⁻¹² M for SEQ ID NO: 96, 3.4±0.28×10⁻¹³ M for SEQ ID NO: 102 and 5.8±1.5×10⁻¹² M for SEQ ID NO: 98.

FIG. 11: Biochemical characterization of N-glycosylated polypeptide according to the present invention (SEQ ID NO: 98). (A) SEQ ID NO: 98 was treated with N-glycosidase and analysed by SDS-PAGE and Coomassie staining. (B) SEQ ID NO: 98 and SEQ ID NO: 96 were separated by size exclusion chromatography on a BioSuite 450 column (Waters). The retention times of the molecular weight standards apoferritin (443 kDa), β-amylase (200 kDa), bovine serum albumin (67 kDa) and carbonic anhydrase (29 kDa) were indicated by dotted lines.

FIG. 12: Receptor interaction of EGFR-specific TRAIL fusion proteins. (A) Dose response relationship of TRAIL fusion protein binding to EGFR⁺ NCI-H460 cells by indirect immunofluorescence flow cytometry to reveal concentration of half maximum binding (EC₅₀) (mean SEM, n=4). (B) Colo205 and Huh-7 cells were serum-starved overnight and then incubated with 2 nM of SEQ ID NO: 102, Cetuximab, and PBS for control, respectively. After 10 min, 50 ng/ml EGF were added and cells were incubated for additional 20 min followed by cell lysis. EGF receptors were immunoprecipitated using a specific mouse monoclonal antibody and subjected to SDS-PAGE followed by immunoblotting with phosphotyrosine antibody (anti-pTyr). Total amounts of EGFR were determined by reprobing the membrane with EGFR-specific rabbit polyclonal antibody (anti-EGFR).

FIG. 13: Caspase dependence of cell death and impact of the component B of SEQ ID NO: 102. (A) Colo205 cells (left) and Huh-7 cells (right) were sensitized with 25 ng/ml and 250 ng/ml bortezomib, respectively, and treated with different concentrations of SEQ ID NO: 102 with or without the presence of pan-caspase inhibitor zVADfmk or caspase-3 inhibitor zDEVDfmk (both inhibitors: 20 μM for Colo205 and 10 μM for Huh-7). After 16 h, cell viability was determined using MTT staining (Colo205) or crystal violet staining (Huh-7) and data were normalized using bortezomib-treated cells as control (mean SEM, n=3). (B) 1×10⁴ Colo205 cells per well were grown in 96-well plates using medium with 0.1% FCS. Upon stimulation with 50 ng/ml EGF and sensitization with 10 ng/ml bortezomib, cells were incubated with equimolar concentrations of SEQ ID NO: 102 (open squares), SEQ ID NO: 102+anti-TRAIL mAb 2E5 (filled squares) or Cetuximab (circles) for four days and cell number was assayed by the MTT method using bortezomib/EGF-treated cells as control for normalization (mean SEM, n=2). (C) 1×10⁴ Huh-7 cells per well were grown in 96-well plates and treated with 20 ng/ml bortezomib or with a combination of bortezomib and 10 μM zVADfmk. Then, cells were incubated with equimolar concentrations of SEQ ID NO: 102 (open squares), SEQ ID NO: 102+zVADfmk (filled squares), Cetuximab (open circles) or Cetuximab+zVADfmk (filled circles) for three days and cell viability was assayed by the MTT method using bortezomib-treated cells and bortezomib/zVADfmk-treated cells, respectively, as control for normalization (mean SEM, n=3).

FIG. 14: In vitro tolerance of TRAIL fusion proteins to primary tissues. (A) Relative caspase activity (fold increase compared to untreated) in primary human hepatocytes (PHH, mean SEM, n=5) or Huh-7 hepatocarcinoma cells (mean SEM, n=7) after incubation with 1.1 nM SEQ ID NO: 102 in presence or without 500 ng/ml bortezomib. Asterisks indicate statistical significance. (B) Cleavage of caspase-3 in PHH (left) and Huh-7 cells (right) after incubation with 500 ng/ml bortezomib, 1.1 nM SEQ ID NO: 102 or both was analyzed by immunoblotting.

FIG. 15: Antitumor activity of TRAIL fusion proteins in a Colo205 xenograft tumor model. (A) Tumor volume as a function of time after i.p. application of PBS (open diamonds), bortezomib (filled triangles), SEQ ID NO: 104 (lacking component B)+bortezomib (open triangles), SEQ ID NO: 97 (L>12 amino acids)+bortezomib (circles), SEQ ID NO: 102 (L<12 amino acids)+bortezomib (filled diamonds) or SEQ ID NO: 102 only (squares). Arrows, protein application; asterisks, bortezomib application; symbols, mean of tumor volumes 95% confidence interval (CI), n=12 tumors/treatment group. (B) Individual tumor volumes at day 14. Bars, mean of tumor volumes 95% CI.

FIG. 16: Coomassie-stained SDS-PAGE of affinity-purified SEQ ID NO: 102 (lane 1), SEQ ID NO: 125 (lane 2) and SEQ ID NO: 126 (lane 3). 5 μg of the proteins were loaded under reducing conditions.

FIG. 17: Albumin binding of SEQ ID NO: 125 and SEQ ID NO: 126. Both proteins were incubated for 1 h at RT with equimolar concentrations of human serum albumin (HSA) or mouse serum albumin (MSA) and subsequently separated by size exclusion chromatography. Thyroglobulin (669 kDa), apoferritin (443 kDa), -amylase (200 kDa), bovine serum albumin (67 kDa), carbonic anhydrase (29 kDa) and FLAG peptide (1 kDa) were used as standard proteins/peptides.

FIG. 18: Bioactivity of SEQ ID NO: 125 and SEQ ID NO: 126 in vitro. Huh-7 hepatocarcinoma cells were sensitized with bortezomib (250 ng/ml) and treated with serial dilutions of SEQ ID NO: 102, SEQ ID NO: 125 (left panel) and SEQ ID NO: 126 (right panel) in triplicates. After 16 h, cell viability was determined using crystal violet staining. For quantification of the targeting effect, cells were preincubated with an excess of Cetuximab (70 nM) before adding SEQ ID NO: 102, SEQ ID NO: 125 and SEQ ID NO: 126. SEQ ID NO: 125 and SEQ ID NO: 126 were additionally incubated in presence of 100 μg/ml HSA. The values for SEQ ID NO: 102 were plotted in both panels for comparison.

FIG. 19: Pharmacokinetics of SEQ ID NO: 102 (A) and SEQ ID NO: 125 (B). 25 μg of protein were injected i.v. in CD1 mice and serum samples were taken at the depicted time points followed by detection of scTRAIL molecules via ELISA.

FIG. 20: Sequence of SEQ ID NO: 96.

FIG. 21: Sequence of SEQ ID NO: 102.

FIG. 22: Sequence of SEQ ID NO: 97.

FIG. 23: Sequence of SEQ ID NO: 98.

FIG. 24: Sequence of SEQ ID NO: 103.

FIG. 25: Sequence of SEQ ID NO: 125.

FIG. 26: Sequence of SEQ ID NO: 126.

FIG. 27: Sequence of SEQ ID NO: 127.

FIG. 28: Sequence of SEQ ID NO: 128.

FIG. 29: Sequence of SEQ ID NO: 129.

EXAMPLES

In the following, general examples illustrating various embodiments and aspects of the invention are presented. However, the present invention shall not be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become readily apparent to those skilled in the art from the foregoing description, accompanying figures and the examples below. All such modifications fall within the scope of the appended claims.

Example 1: Biochemical Analysis 1. Polypeptide Production 1.1 Principle

Three human TRAIL domains encompassing aa residues 95-281 (TRAIL) (SEQ ID NO: 5) were fused with (GGGS)₂ peptide linkers P (SEQ ID NO: 48) yielding so called single-chain TRAIL (scTRAIL) (SEQ ID NO: 104). EGFR-specific antibody fragments consisting of V_(H) (SEQ ID NO: 93) and V_(L) (SEQ ID NO: 92) were fused N-terminally to scTRAIL (SEQ ID NO: 104). (GGGGS)₃ (SEQ ID NO: 52) or GGGGS (SEQ ID NO: 50) peptide linkers between V_(H) (SEQ ID NO: 93) and V_(L)(SEQ ID NO: 92) were chosen to obtain a polypeptide according to the present invention (SEQ ID NOs: 96 and 102). A V_(H) leader (K) (SEQ ID NO: 101) and a FLAG tag (F) (SEQ ID NO: 100) were placed in front of the antibody region. For a glycosylated polypeptide according to the present invention, a linker with two N-glycosylation sites (GNGTSNGTS) (SEQ ID NO: 83) was placed between V_(L) (SEQ ID NO: 92) and scTRAIL (SEQ ID NO: 104).

1.2 Plasmids and Cell Lines

An pIRESpuro-scTRAIL expression construct for human scTRAIL (SEQ ID NO: 104) was obtained by EcoRI/NotI cloning of a synthesized sequence coding for three TRAIL components (aa residues 95-281) connected by sequences encoding (GGGS)₂ linker motifs into a construct described previously (Schneider et al, 2010, Cell Death. Disease. 2010). For the generation of the EGFR-specific V_(H)-V_(L)-scTRAIL expression construct, a synthesized coding sequence of humanized V_(H) and V_(L) sequences (huC225) was amplified using the oligonucleotides CGAGGTGCAGCTGGTCGAG (SEQ ID NO: 109) and TGCGGCCGCTCTCTTGATTTC (SEQ ID NO: 110). Next, this template was annealed with the oligonucleotide ATATATCTCGAGGCCAGCGACTACAAAGACGATGACGATAAAGGAGCCGAGGTGCAGCTGG TCGAG (SEQ ID NO: 111) to insert an XhoI site and a FLAG tag coding sequence. After strand elongation, the whole sequence was amplified by the oligonucleotides ATATATCTCGAGGCCAGCGAC (SEQ ID NO: 112) and ATATGAATTCTGCGGCCG CTCTCTTGATTTC (SEQ ID NO: 113). The PCR product was then cloned via XhoI/EcoRI into pCR3 (Invitrogen), carrying an V_(H) leader. The scTRAIL coding sequence of this construct was then inserted via EcoRI/XbaI sites. The EGFR-specific construct for SEQ ID NO: 102 was derived from pCR3-VH-VL-scTRAIL by shortening linker L from (GGGGS)₃ to GGGGS. Therefore, two PCR products were generated using the oligonucleotide

(1) (SEQ ID NO: 114) CCCACAGCCTCGAGGCCAG and (2) (SEQ ID NO: 115) GAGCCGCCACCGCCACTAG vas well as

(3) (SEQ ID NO: 116) CTAGTGGCGGTGGCGGCTCTGATATTCAGCTGA CCCAGTCC and (4) (SEQ ID NO: 117) TGAATTCTGCGGCCGCTCTC. After annealing of the products at the underlined regions and strand elongation, the whole sequence was amplified by the oligonucleotides (1) and (4) followed by XhoI/NotI cloning into pCR3-V_(H)-V_(L)-scTRAIL. A glycosylated variant of SEQ ID NO: 96 was generated by two PCR amplifications of the huC225 VH-VL coding sequence in pCR3-VH-VL-scTRAIL using the oligonucleotides (1) CCCACAGCCTCGAGGCCAG (SEQ ID NO: 118) and CCCGTTGCTGGTGCCGTTGCCTGCG GCCGCTCTCTTG (SEQ ID NO: 119), respectively (1) and ATATGAATTCGGATGTCCCGTT GCTGGTGCCGTTG (SEQ ID NO: 120), followed by XhoI/EcoRI cloning in pCR3-VH-VL-scTRAIL. The construct for expression of SEQ ID NO: 98 was generated by two sequential PCR amplifications of the TRAIL coding sequence using the oligonucleotides GCACATCCAATGGGACCAGCGGAACCTCCGAAGAGACTATCTC (SEQ ID NO: 121) and CCCGTTGCTGGTTCCATTACCAGATCCGCCCCCTCC (SEQ ID NO: 122), respectively ATATATGGATCCGGCAACGGCACATCCAATGGGACCAG (SEQ ID NO: 123) and ATATATGGATCCGGTCCCGTTGCTGGTTCCATTAC (SEQ ID NO: 124), followed by BamHI cloning into the expression construct for SEQ ID NO: 97.

HEK293, HepG2, NCI-H460, Colo205 and Jurkat, cells were obtained from the American Type Culture Collection (Manassas, Va.). Cells were cultured in RPMI 1640 medium (Invitrogen, Karlsruhe, Germany) supplemented with 5% fetal calf serum (FCS, HyClone), respectively 10% FCS for HepG2. Huh-7D12 liver carcinoma cells were obtained from Heike Bantel, Hannover Medical School, Hannover, Germany and were cultured in DMEM (Invitrogen, Karlsruhe, Germany) supplemented with 10% FCS.

1.3 Production and Purification of Recombinant Proteins

The TRAIL fusion proteins of SEQ ID NOs: 96, 97, 98, 102, 125, and 126 were produced in HEK293 cells after stable transfection with the corresponding expression plasmids using Lipofectamine 2000 (Invitrogen) and generation of a pool of stably expressing clones. For protein production, stable clones were expanded and grown in RPMI 1640, 5% FCS, to 90% confluency and subsequently cultured in serum-free Optimem (Invitrogen) supplemented with 50 μM ZnCl₂, replacing media two times every 3 days. The supernatants were pooled and recombinant proteins were purified first by IMAC using Ni-NTA-Agarose (Qiagen, Hilden, Germany). After elution with 100 mM imidazol and dialysis against PBS, the proteins were further purified by affinity chromatography using anti-FLAG mAb M2 agarose (Sigma-Aldrich, Steinheim, Germany). The bound proteins were eluted with 100 μg/ml FLAG peptide (peptides&elephants, Potsdam, Germany) and dialysed against PBS. scTRAIL and SEQ ID NOs: 97 and 98 were purified in a single M2 agarose affinity chromatography step. After concentration of purified proteins using Vivaspin centrifugal concentrators with 50 or 10 kDa MWCO (Sartorius Stedim, Aubagne, France), the protein concentration was measured with a spectrophotometer (NanoDrop products, Wilmington, Del.) and aliquots were stored at −80° C.

1.4 SDS-PAGE and Western Blot Analysis

Purified polypeptides of SEQ ID NO: 96, SEQ ID NO: 102, SEQ ID NO: 104, 125, 126 and of glycosylated SEQ ID NO: 97 were analyzed by SDS-PAGE (reducing conditions) followed by silver staining (1 μg protein per lane), Coomassie staining or Western blotting (250 ng protein per lane) using monoclonal anti-TRAIL (MAB687, R&D Systems, Wiesbaden, Germany) or anti-FLAG antibodies (M2, Sigma-Aldrich) in combination with alkaline phosphatase-conjugated secondary antibody (Sigma-Aldrich). The glycosylated polypeptide of SEQ ID NO: 97 was treated with N-glycosidase and analysed by SDS-PAGE and Coomassie staining. For deglycosylation, protein (5 μg) was denatured in the presence of SDS and DTT prior to addition of Nonidet P-40 and 500 units of PNGaseF (New England Biolabs, Frankfurt a. M., Germany) according to the supplier's instructions. After 1 h incubation at 37° C., samples were subjected to SDS-PAGE. For Western blotting, an anti-TRAIL antibody MAB687 (R&D Systems, Wiesbaden, Germany) and anti-FLAG M2 mAb (Sigma-Aldrich) were used, followed by an anti-mouse alkaline phosphatase-coupled secondary antibody (Sigma-Aldrich) for detection.

The results of the SDS PAGE/Western Blot analysis verified the increase in molecular mass of SEQ ID NOs: 96, 97 and 102 vs. SEQ ID NO: 104. The increase of molecular mass of SEQ ID NOs: 125 and 126 vs. SEQ ID NO: 102 has been verified by SDS page and Coomassie staining. SEQ ID NO: 97 showed reduced migration in SDS PAGE, which is conform with effective glycosylation of the protein. This was confirmed by PNGaseF treatment of the fusion protein, which removes carbohydrate side chains in glycoproteins, resulting in a shift of the specific band towards the mass of the non-glycosylated form. Furthermore, the assays confirmed the presence of TRAIL as well as of the FLAG-tag in all 4 polypeptides.

1.5 Size Exclusion Chromatography and Albumin Binding Assay

Purified polypeptides of SEQ ID NO: 96, SEQ ID NO: 102, SEQ ID NO: 104 and of glycosylated SEQ ID NO: 97 were separated by size exclusion chromatography on a BioSuite 250 HR SEC (300×7.8) column (Waters, Millipore Corp., Milford, Mass.) equilibrated in PBS and eluted at a flow rate of 0.5 ml/min.

Albumin binding to the polypeptides of SEQ ID NOs: 125 and 126 has been verified by incubating the polypeptides with human serum albumin or mouse serum albumin and determining protein-protein interaction by size exclusion chromatography as described above.

1.6 Immunoprecipitation and Protein Analysis

For immunoprecipitations, cells were lysed on ice in RIPA buffer (50 mM Tris, pH 7.5, 150 mM NaCl, 10 mM sodium fluoride, 20 mM glycerophosphate, 1 mM EDTA, 1% NP40, 1 mM sodium orthovanadate, 0.5 mM phenylmethylsulfonyl fluoride, 0.1% SDS, 0.25% sodium deoxycholate) with Complete protease inhibitor (Roche Diagnostics, Mannheim, Germany) and lysates were clarified by centrifugation (16 000 g, 10 min, 4° C.). 1.5 mg lysate protein was incubated with 1.5 μg mouse anti-EGFR Ab-13 mAb (Neomarkers, Fremont, Calif., USA) under gentle shaking at 4° C. overnight. Immune complexes were captured with protein G sepharose (KPL, Gaithersburg, Md., USA) and washed three times with RIPA buffer. Proteins were analyzed by SDS-PAGE and Western blotting using mouse anti-phosphotyrosine P-Tyr-100 mAb (Cell Signaling Technology, Danvers, Mass., USA) and rabbit anti-EGFR 1005 antibody (Santa Cruz Biotechnology, Santa Cruz, Calif., USA) followed by HRP-conjugated secondary antibodies. ECL (Pierce Biotechnology, Rockford, Ill., USA) was used for visualization.

Caspases were detected by immunoblotting using a rabbit polyclonal antibody against cleaved caspase-3 (Cell Signaling Technology). GAPDH as internal control was detected with a rabbit polyclonal antibody (Cell Signaling Technology). HRP-conjugated secondary antibodies (Zymed Laboratories, San Fransisco, Calif., USA) and ECL were used for visualization.

Example 2: Flow Cytometry, Cell Death Assay, ALT and Caspase Activities 2.1 Flow Cytometry

5×10⁵ cells were suspended in PBA buffer (PBS, 0.025% BSA, 0.02% sodium azide) and incubated for 1 h at 4° C. with the indicated scTRAIL fusion proteins (2 μg/ml). After washing the cells three times with PBA buffer, bound fusion proteins were detected by anti-human TRAIL mAb MAB687 (2.5 μg/ml, R&D Systems) and fluorescein isothiocyanate-labelled rabbit anti-mouse IgG Ab (1:200, Sigma-Aldrich), followed by three washing steps with PBA each. For blocking of scTRAIL fusion protein binding to EGFRs (see FIG. 5B), a divalent variant of huC225 (huC225Cys, 50 μg/ml, kindly provided by Celonic GmbH, Jülich, Germany) was added 30 min before addition of SEQ ID NO: 96 and SEQ ID NO: 102, respectively. Expression of TRAIL receptors was detected by anti-TRAIL R1 mAb MAB347 and anti-TRAIL R2 mAb MAB6311 (4 μg/ml each, R&D Systems) in conjunction with anti-mouse IgG-FITC. EGFR expression was detected by a phycoerythrin-labelled anti-human EGFR mAb sc-101 (4 μg/ml, Santa Cruz Biotech., Santa Cruz, Calif.) (see FIG. 4). For binding inhibition, purified SEQ ID NO: 102 (50 μg/ml) was added 30 min prior addition of Alexa Fluor 488-coupled mAb Cetuximab (1 μg/ml) (see FIG. 5A).

The assays determined the expression levels of EGF receptor and proapoptotic TRAIL receptors DR4 and DR5 in Huh-7 and Hep2G hepatocellular carcinoma cell lines and the T cell leukemia line Jurkat, revealing Huh7 as EGFR+, DR4+, DR5 low; HepG2 as EGFR low/negative, DR4+, DR5+; and Jurkat as EGFR negative, DR4 negative, DR5 low (see FIG. 4). Furthermore, blocking of the binding of anti EGFR mab Cetuximab to EGFR+ cells (Huh-7) by an excess of EGFR receptor specific TRAIL protein (SEQ ID NO: 102) revealed functional expression of the EGFR specific V_(H)-V_(L) domain within the fusion protein of SEQ ID NO: 102 (FIG. 5A, right panel); as expected, the marginal Cetuximab staining of EGFR low/negative HepG2 cells could not be further reduced by an excess of the fusion protein of SEQ ID NO: 102, and likely reflect nonspecific background staining of the reagent. Likewise, binding of the EGFR targeting fusion proteins SEQ ID NO: 102 and SEQ ID NO: 96 to EGFR+ Huh-7 cells was partially blockable by an excess of an anti-EGFR specific antibody fragment, whereby the remaining signal could be attributed to specific binding of the fusion proteins via the TRAIL domain to their cognate TRAIL receptors. In this experimental setting, binding of fusion proteins was clearly discernable for DR4+DR5+HepG2 cells, too, with little blocking of the signal by addition of an anti-EGFR specific antibody fragment due to low expression of EGFRs at or below the detection level in these cells.

2.2 Cell Death Assays

Huh-7 (3×10⁴), HepG2 (3×10⁴), Colo205 (5×10⁴ per well) or Jurkat cells (1×10⁵) were grown in 100 μl culture medium in 96-well plates for 24 h, followed by treatment with the indicated concentrations of SEQ ID NOs: 96, 102, 125, 126 and 104 or ‘KillerTRAIL’ (Axxora Deutschland GmbH, Lörrach, Germany) in triplicates (see FIGS. 6-8 and 18). As a positive control, cells were killed with 0.25% Triton X-100. Cell death assays with Huh-7 and HepG2 cells were performed in the absence (FIG. 6, Jurkat cells) or presence of Bortezomib (FIG. 7, Huh-7: 250 ng/ml, FIG. 6, HepG2: 500 ng/ml, FIG. 18, Huh-7: 250 ng/ml), Selleck Chemicals, Houston, Tex.). Bortezomib was added 30 min prior incubation with the proapoptotic ligands to sensitize cells for the induction of cell death (FIGS. 6, 7). Alternatively, cells were preincubated for 30 min with the indicated concentrations of TRAIL fusion proteins followed by addition of serial dilutions of Bortezomib (FIG. 8). TRAIL only treated cells are shown in each panel for the applied TRAIL concentration (Bortezomib 0 ng/ml) (FIG. 8). After 16 h incubation, cell viability was determined either by crystal violet staining (Huh-7, HepG2) or the MTT method (Jurkat) (Wuest et al., 2002). In the latter case a lysis buffer consisting of 15% SDS in DMF/H₂O (1:1), pH 4.5 (with 80% acetic acid) was used. To demonstrate target antigen-dependent induction of cell death, cells were preincubated for 30 min with competing Cetuximab mAb (10 μg/ml, Merck, Darmstadt, Germany) (FIG. 18) or alternatively EGFR specific huC225Cys (10 μg/ml) (FIG. 7).

2.3 Alanine Aminotransaminase (ALT) and Caspase Activities

Groups of three CD1 mice (Janvier, Le Genest-St-Isle, France) were treated i.p. with 1 nmol of fusion proteins according to SEQ ID NO: 102 and SEQ ID NO: 97, 0.1 nmol FasL fusion protein (positive control) and PBS (negative control), respectively. Blood samples were taken from the tail after 4 h and 24 h and incubated on ice. Clotted blood was centrifuged (10 000 g, 10 min, 4° C.) and serum samples were stored at −80° C. Activity of alanine aminotransaminase was determined by an enzymatic assay (BIOO Scientific, Austin, Tex., USA). To determine caspase-3 activity in the liver tissue, mice were sacrificed after 24 h (positive control after 5 h) and liver biopsies were taken. Homogenates were prepared in lysis buffer (200 mM NaCl, 20 mM Tris, 1% NP-40, pH 7.4). 10 μg of protein were analyzed by conversion of the fluorogenic substrate Ac-DMQD-AMC (Enzo Life Sciences). Caspase activity in PHH and Huh-7 cells was determined as published by Seidel et al. (Hepatology 2005, 42:113-120).

Example 3: Xenograft Mouse Tumor Model

8-week-old female NMRI nu/nu mice (Janvier) were injected s.c. with 3×10⁶ Colo205 cells in 100 μl PBS at left and right dorsal sides. Treatment started 6 days after tumor cell inoculation when tumors reached about 100 mm³. Mice received 8 daily i.p. injections of 0.45 nmol of the affinity-purified TRAIL fusion proteins according to SEQ ID NOs: 104, 97, and 102, respectively. On day 1, 3, 5 and 7 of treatment, mice received additionally 5 μg bortezomib in 100 μl PBS i.p. three hours before protein injection. The control groups received 100 μl PBS or 5 μg bortezomib at the same time intervals. Tumor growth was monitored as described in Schneider et al. (Cell Death Dis. 2010; 1: e68) and Kim et al. (Bioconjug. Chem. 2011; 22: 1631-1637). The Tukey's test was applied for statistics.

Description of Results Disclosed in Examples 1, 2 and 3

The main aim of the shown examples was the improvement of the proapoptotic activity of scTRAIL fusion proteins under retention of their tumor selectivity, i.e. non-reactivity towards normal, non-malignant tissue. In principle, the same rules apply for other proapoptotic members of the TNF family, as well as all other non-apoptotic, tissue and immune-regulatory TNF ligands that are inactive as soluble ligands or require membrane targeting to restrict their activity to the relevant tissue or cell types. The examples are also not restricted to the specific target antigen used exemplarily (EGFR), but apply, in principle, to all other tissue or cell selective targets, including, for tumor therapeutic purposes, tumor stroma markers such as fibroblast activation protein.

Construction and Preparation of scTRAIL Fusion Proteins

For generation of functionally improved scFv-TRAIL fusion proteins, first, the genetic code of scTRAIL was adapted for higher protein yields in mammalian expression systems. Among the various linker motifs suitable to connect 3 Trail molecules (components A) the (GGGS)1-4 motifs were tested, with the shorter linkers (GGGS)₁ (SEQ ID NO: 47) and (GGGS)₂ (SEQ ID NO: 48) being superior to longer linkers with respect to protein stability, tendency to aggregate and display identical or better apoptosis inducing activity.

The inventors used EGFR targeting as a model system. Like other members of the erbB family of receptor tyrosine kinases, the EGFR (erbB1) is an established tumor marker, which is overexpressed in several carcinomas, including lung and liver cancer (Olayioye et al, 2000). For generation of the EGFR specific fusion protein of SEQ ID NO: 96, the construct was N-terminally fused with component B, a humanized and codon-optimized antibody fragment derived from the anti-EGFR mAb Cetuximab (C225) (Naramura et al, 1993) (SEQ ID NO: 94). A FLAG tag (F) was placed N-terminal of component B for purification and detection purposes (FIG. 1A). TRAIL bioactivity depends on the oligomerization state, in particular relevant for TRAILR2 (DR5), which is poorly activated by soluble, trimeric forms of TRAIL (Wajant et al, 2001). For SEQ ID NO: 102 the linker L between V_(H) and V_(L) was shortened from (GGGGS)₃ (SEQ ID NO: 52) to GGGGS (SEQ ID NO: 50). In an independent approach to improve basal protein stability and protection from proteolytic processing during expression culture conditions, two variants of SEQ ID NO: 96 were designed, in which i) the linker X connecting component A and B comprised two N-glycosylation sites, yielding a monomeric glycosylated form (SEQ ID NO:97) and ii) in addition, the two glycin linkers (P) connecting the three TRAIL components were replaced by linkers (P1, P2) each comprising two N-glycosylation sites, too (FIG. 1) (SEQ ID NO: 98).

Following expression in stably transfected HEK293 cells, the purification of SEQ ID NO: 96 and SEQ ID NO: 102 was accomplished both by IMAC due to intrinsic histidine residues of TRAIL and by M2 mAb affinity chromatography. For example, yields of >3 mg highly pure protein per liter cell culture supernatant were achievable for both fusion proteins. SDS-PAGE and Western blot analysis of the purified proteins revealed single protein bands with an approx. molecular mass of 70 kDa and 100 kDa for scTRAIL (SEQ ID NO: 104) and EGFR specific V_(H)-V_(L)-scTRAIL fusion proteins SEQ ID NOs: 96 and 102, respectively, matching the expected calculated molecular masses of the single stranded monomers of 68, 93 and 94 kDa (FIG. 2). The apparent molecular mass of SEQ ID NO: 97 was increased compared to SEQ ID NO: 96, in accordance with effective glycosylation of the introduced linker. N-glycosidase treatment of SEQ ID NO: 97 resulted in a protein with a molecular mass essentially identical to that of its non-glycosylated derivative. The introduction of N-glycosylation sites in SEQ ID NO: 96 improved protein stability and protection from degradation during the production process, evident from strong reduction of degradation products present in culture supernatants (not shown). This allows a single-step purification of glycosylated variants such as SEQ ID NO: 97 with M2 agarose to gain a purification grade comparable to that of non-glycosylated fusion proteins after a two-step purification and thus overall higher yields of purified, bioactive protein.

The gel filtration analysis of fusion proteins (SEQ ID NO: 104) and SEQ ID NO: 96 (both, with and without glycosylation) indicated that the majority of protein (>94%) exists as a monomer (FIG. 3), whereas retention times decrease from scTRAIL (SEQ ID NO: 104) to SEQ ID NO: 97, according to the increase in molecular size. Concerning scTRAIL (SEQ ID NO: 104), the molecular mass deduced from SEC was slightly lower compared to that calculated from SDS-PAGE (FIG. 2), which is a characteristic of this molecule and not a hint for degradation (Schneider et al, 2010). Interestingly, SEC of SEQ ID NO: 102 revealed the presence of two peaks. The major peak near 200 kDa could be attributed to a dimer, whereas the minor peak could represent trimeric and/or tetrameric forms of the fusion protein.

TRAIL fusion proteins comprising an albumin binding domain (ABD) either between component A and component B (SEQ ID NO: 125) or at the C-terminus of the fusion protein (SEQ ID NO: 126) have been purified from HEK293 cells as described above. The increase in molecular weight, which is essentially the result of the introduction of the ABD, can be seen on the Coomassie stained SDS-PAGE gel depicted in FIG. 16.

Size exclusion chromatographie experiments showed that the TRAIL fusion proteins comprising an albumin binding domain are indeed capable of binding both, humen and mouse serum albumin (FIG. 17).

EGFR-Specific Binding of scTRAIL Fusion Proteins

The specific antigen binding of various scTRAIL fusion proteins to EGFR-positive cells was analysed by flow cytometry of two HCC cell lines. Whereas EGFRs in HepG2 cells were barely detectable and thus considered target antigen low/negative, EGFR expression was clearly revealed in Huh-7 cells (FIG. 4), although EGFR levels in this HCC line appear moderate compared with EGFR overexpressing A431 cells (data not shown). Consistent with this, the binding of labelled Cetuximab to the EGFR-positive Huh-7 cells can be blocked by preincubation with 0.5 μM of SEQ ID NO: 102 (FIG. 5). Incubation of HepG2 and Huh-7 cells with SEQ ID NO: 96 or SEQ ID NO: 102 resulted in binding of the proteins to both cell lines, but competition of fusion protein binding by preincubation of cells with the anti-EGFR huC225 (2 μM) was only possible on Huh-7 cells (FIG. 2C). The intermediate fluorescence signal observed upon competition of fusion protein binding to Huh-7 cells likely reflects binding of the TRAIL domain (component A of the fusion protein) to TRAIL receptors. This is consistent with the weaker and non-blockable binding of SEQ ID NO: 96 and SEQ ID NO: 102 on EGFR low/neg. HepG2 cells. Binding competition of both fusion proteins to EGFR-positive cells is an indicator for the structural integrity and functionality of the targeting domain (component B).

Quantitative binding studies of TRAIL fusion proteins to EGFR+, DR4+5+ NCI-H460 cells revealed significantly different (P=0.003) EC50 values for TRAIL fusion protein according to SEQ ID NO: 97 (3.6±0.3×10⁻¹⁰ M) and TRAIL fusion protein according to SEQ ID NO: 102 (1.6±0.3×10⁻¹⁰ M), implicating an avidity effect of the specific molecular composition of the divalent TRAIL fusion protein according to SEQ ID NO: 102 and therefore potentially superior targeting compared to TRAIL fusion protein according to SEQ ID NO: 97 (FIG. 12A). Furthermore, it has been investigated whether the TRAIL fusion protein according to SEQ ID NO: 102 exhibits the functional activity of blocking EGF-induced EGFR autophosphorylation. Cetuximab served as a positive control in this experiment. Functional blocking of EGF-stimulated receptor activation by the divalent TRAIL fusion protein according to SEQ ID NO: 102 could be demonstrated for both Colo205 (FIG. 12B, left panel) and Huh7 (FIG. 12B, right panel) cells.

Target-Independent Induction of Cell Death by scTRAIL Fusion Proteins

To investigate the basic bioactivity of scTRAIL fusion proteins without the influence of targeting domains, we first analysed cell death induction on the target-negative cell lines HepG2 (hepatoma) and Jurkat (T cell leukemia) and compared it with a non targeting scTRAIL molecule. On all cell lines analysed, SEQ ID NO: 102 exerted an approximately tenfold increased bioactivity compared to SEQ ID NO: 96 or its glycosylated form (SEQ ID NO: 97). As a reference, the bioactivity of a commercially available highly active TRAIL preparation, so-called ‘KillerTRAIL’(Enzo Lifesciences), was found to be comparable with the activity of SEQ ID NO: 96. Due to the low or even deficient target antigen expression of HepG2 cells, the apoptosis inducing activity of SEQ ID NO: 102 and SEQ ID NO: 96 was not influenced by the presence of an at least 7-fold excess (70 nM) of Cetuximab (not shown). The bioactivity of SEQ ID NO: 96 on target negative cells did not differ from the one of SEQ ID NO: 104 (scTRAIL). On EGFR-negative, DR4-DR5^(weak) Jurkat cells, which are known to be sensitive for apoptosis induced by TRAIL complexes but not by soluble TRAIL, we found a higher apoptosis-inducing activity of SEQ ID NO: 102 compared to KillerTRAIL and no reactivity towards the SEQ ID NOs: 96 and 104 (FIG. 6).

EGFR-Directed Enhancement of Cell Death by scTRAIL Fusion Proteins

The EGFR-positive liver carcinoma cell line Huh-7 was chosen to demonstrate the enhancement in bioactivity achievable due to the receptor targeting capacity of SEQ ID NO: 96 and SEQ ID NO: 102. Compared to scTRAIL (SEQ ID NO: 104), SEQ ID NO: 96 showed tenfold better apoptosis-inducing activity on Huh-7 cells (FIG. 7). The competition of this bioactivity with an excess of Cetuximab (70 nM) revealed a right shift of EC50 of SEQ ID NO: 96 in the same order of magnitude, pointing to the functionality of EGFR targeting responsible for the improvement of scTRAIL bioactivity. Glycosylated SEQ ID NO: 97 exerted identical bioactivity compared to its non-glycosylated variant, indicating that glycosylation at this site did not impact bioactivity. SEQ ID NO: 102 showed a tenfold enhanced bioactivity in relation to SEQ ID NO: 96. The competition of activity of SEQ ID NO: 102 with the same molar excess of Cetuximab also resulted in a comparable shift in the dose response curve, confirming that targeting further improves the already increased bioactivity of this fusion protein. Furthermore, dimeric TRAIL fusion proteins comprising an albumin binding domain (ABD) (SEQ ID NOs: 125 and 126) exhibited bioactivity comparable to the dimeric TRAIL fusion protein lacking an ABD (SEQ ID NO: 102) indicating that the introduction of an ABD as performed for TRAIL fusion proteins according to SEQ ID NOs: 125 and 126 does not significantly influence the bioactivity of EGFR-directed enhancement of cell death (FIG. 18).

In another experimental setup, Huh-7 cells were pretreated with a fixed dose of the various TRAIL fusion proteins followed by titration of the apoptosis sensitizer Bortezomib (FIG. 8). At a protein concentration of 1 nM and above, the tested SEQ ID NOs: 102, 96 and 104 were nearly equally efficient in induction of complete apoptosis in these cells when sensitized with Bortezomib. In contrast, at protein concentrations of 0.1 nM and below, a strong synergistic effect of Bortezomib sensitization and the EGFR targeting ability of the constructs became visible. At a protein concentration of 0.05 nM, only SEQ ID NOs: 96 and 102 were able to synergize with Bortezomib, whereby SEQ ID NO: 102 showed higher bioactivity compared to SEQ ID NO: 96 at this concentration. Superior activity of SEQ ID NO: 102 was even more apparent at 0.01 nM of fusion proteins (FIG. 8).

A nearly complete block of cell death by either pan-caspase (zVADfmk) or caspase-3 selective (zDEVDfmk) inhibitors (FIG. 13A) and failure of necrostatin-1 to prevent or reduce cell death (data not shown) indicated that Huh-7 and Colo205 undergo predominantly apoptotic cell death upon treatment with TRAIL fusion proteins. Cetuximab blocked EGF-induced autophosphorylation of EGF receptors (FIG. 12B). Further, cetuximab by itself, though blocking EGF-induced autophosphorylation of EGFR in Colo205 and in Huh7 cells (FIG. 12B), did not substantially affect growth of these two cancer cell lines in a 4-day culture (FIG. 13B, C). Likewise, when SEQ ID NO: 102-induced apoptosis was prevented, either by presence of neutralizing anti-TRAIL antibodies in SEQ ID NO: 102 treated Colo205 cell cultures (FIG. 13B) or by treating Huh-7 cell cultures with pan-caspase inhibitors (FIG. 13C), only a marginal growth inhibition was noted during the 4 day observation period. Together, for the cells and the in vitro conditions studied here, the data indicate that i) SEQ ID NO: 102-induced cell death requires TRAIL signaling and ii) blocking EGFR function by the SEQ ID NO: 102 does not contribute to rapid apoptosis induction.

Binding Affinity of SEQ ID NO: 96 and SEQ ID NO: 102 to Cells

The specific molecular composition of SEQ ID NO: 102 implies avidity effects and thus potential superior targeting functions as compared to SEQ ID NO: 96. Therefore, we determined dissociation constants of both fusion proteins on EGFR-positive, DR4+5+ NCI-H460 cells under equilibrium binding conditions at 4° C. by indirect immunofluorescence flow cytometry with an anti-TRAIL antibody. The K_(D) of the interaction between the scTRAIL fusion proteins and NCI-H460 cells at 4° C. was determined by Lineweaver-Burk kinetic analysis (Lineweaver and Burk, 1934; Benedict et al, 1997) and was found to be 4-fold lower for the fusion protein of SEQ ID NO: 102 (6.5±0.9×10⁻⁸ M for SEQ ID NO: 96 and 1.7±1.2×10⁻⁸ M for SEQ ID NO: 102, respectively). In principle, the measured K_(D) values reflect cell surface interactions of both functional domains in the fusion protein, the EGFR targeting domain (Component B) and the TRAIL domain, (components A), with their respective receptors. However, because SEQ ID NO: 102 binding to TRAILR+, EGFR negative cells such as Jurkat resulted in only very weak signals in this assay (data not shown), we reason that the signals revealed for NCI-H460 are largely due to binding of the fusion protein via its V_(H)-V_(L) domain to EGFRs. In fact, under the assay conditions (4° C.) applied, dynamic clustering of TRAILR that could account for stable receptor ligand interactions and thus apparent enhanced affinity is prevented. Therefore, we attribute this increased affinity largely to an avidity effect of the bivalent targeting domain (component B) of this particular fusion protein (SEQ ID NO: 102).

Lack of Systemic Toxicity of SEQ ID NO: 102 and Pharmacokinetics

To assess whether the strongly increased bioactivity of SEQ ID NO: 102 in vitro diminishes the advantageous tumor selectivity of TRAIL, we studied systemic tolerance and effects of in vivo application on the reportedly most sensitive organ concerning untolerable TRAIL side effects, the liver. Groups of 3 CD1 mice were treated intraperitonally with indicated reagents (FIG. 9): neg. control: PBS; pos. control: aggregated FasL fusion protein; SEQ ID NO: 102 and SEQ ID NO: 96 (A) Plasma samples were prepared after 4 h and 24 h and the activity of alanine aminotransferase (ALT) was assayed using an enzymatic assay. Dashed line indicates upper normal level of ALT (35-50 U/L). (B) Mice were sacrificed after 24 h except for pos. control (animals treated with an aggregated FasL fusion protein show phenotypic signs of severe systemic toxicity after 2-4 hrs and die after ˜5 hrs, samples were taken after 4 hrs) and liver biopsies were taken for determination of caspase-3 activity using a specific AMC-coupled peptide substrate. The data clearly show that the SEQ ID NO: 102, despite its strongly increased apoptotic activity in vitro on target positive tumor cell lines (compared to non-targeted scTRAIL and the most active commercially available TRAIL) remains systemically well tolerated at doses up to 3 mg/kg in mouse models. Moreover, biochemical parameters of organ (liver) specific pathology confirm the phenotypic tolerance to this TRAIL fusion proteins, with only a transient marginal increase in ALT values to the upper normal limit 4 hrs after application. Lack of caspase activation and baseline ALT after 24 hrs, when bioactive fusion protein is still detectable in the blood (Tα_(1/2)=2h, Tβ_(1/2) 3h; plasma conc at t=24h: 100 ng/ml with an applied iv dose of 100 μg/animal; proof that SEQ ID NO: 102 maintain tumor selectivity and can be safely applied in vivo.

Furthermore, a comparison of Huh-7 hepatoma cells and primary human hepatocytes (PHH) for caspase-3 activation by SEQ ID NO: 102 in presence of bortezomib showed a strong, bortezomib-dependent caspase-3 activation in the tumor cells, whereas normal liver cells were neither affected by the scTRAIL fusion protein alone nor in combination with bortezomib (FIG. 14A). These results were confirmed by immunoblot analysis of cleaved caspase-3 in Huh-7 and PHH, with no detectable caspase activation in combination treated PHH, whereas robust caspase processing was detectable in sensitive Huh7 carcinoma cells (FIG. 14B).

Antitumoral Activity of SEQ ID NO: 102 in a Xenograft Tumor Model

Given the in vitro data, showing superior bioactivity of the divalent TRAIL fusion protein according to SEQ ID NO: 102 compared with the monovalent TRAIL fusion protein according to SEQ ID NO: 97 or scTRAIL according to SEQ ID NO: 104 in particular at low protein concentrations, eight doses of 0.45 nmol protein were injected i.p. in a daily regimen in combination with bortezomib cotreatment every second day. The systemic treatment started after establishment of solid, vascularized tumors and tumor growth was monitored for 22 days. Bortezomib treatment by itself did not interfere with progressive tumor growth, whereas scTRAIL according to SEQ ID NO: 104 and the monovalent TRAIL fusion protein according to SEQ ID NO: 97 both delayed tumor growth, but at the low dosage applied, did not induce regression of tumors. In contrast, upon treatment with the divalent TRAIL fusion protein according to SEQ ID NO: 102, a strong reduction of tumor size and prolonged survival in all animals, with macroscopically undetectable tumors in 11/12 (+bortezomib) and 9/12 (w/o bortezomib) cases was recorded (FIG. 15). Interestingly, under the treatment conditions applied there was only a slight, but statistically not significant benefit of cotreatment with bortezomib, although at termination of treatment the combination group presented with slower regrowth of tumors (FIG. 15A).

Introduction of an Albumin Binding Domain Increases the In Vivo Half-Life of TRAIL Fusion Proteins

The pharmacokinetics, in particular, the in vivo half-lives for the dimeric TRAIL fusion protein according to SEQ ID NO: 102 lacking an albumin binding domain (ABD) and the dimeric fusion protein comprising an ABD between component A and component B of the TRAIL fusion protein (SEQ ID NO: 125) have been compared. To this end, 25 μg of fusion proteins were injected i.v. in CD1 mice and serum samples were analyzed at certain time points after injection by ELISA assay (FIG. 19). It has been demonstrated that the in vivo serum half-life increases from about 3 hours for the construct without ABD (SEQ ID NO: 102) to about 20 hours for the construct comprising an ABD (SEQ ID NO: 125) (FIG. 19). As indicated above, the constructs comprising an ABD exert a similar bioactivity compared to the constructs lacking an ABD (Figure. 18) indicating that the ABD does not negatively influence bioactivity, but exerts advantageous properties regarding pharmacokinetic properties, such as in vivo serum half-life. Thus, the TRAIL fusion proteins, preferably dimeric TRAIL fusion proteins, as described above comprising an ABD, such as the dimeric TRAIL fusion proteins according to SEQ ID NO: 125 and 126, are particularly preferred embodiments of the polypeptide according to the present invention.

The inventors of the present invention have thus provided evidence for an improved concept in targeted cancer therapy. It may be that polypeptides according to the present invention form oligomers while polypeptides such as SEQ ID NO: 96 remain strictly monomeric. If so, it is surprising that the potential oligomeric structure of the polypeptides according to the present invention does not result in an increased systemic toxicity. The presence of higher-order aggregates in preparations of recombinant TRAIL constructs (e.g. His-TRAIL, crosslinked FLAG-TRAIL) has been reported previously to be responsible for an increased toxicity towards some non-malignant tissue cells (reviewed by Koschny et al, 2007). Thus, the inventors provide new formats of highly active and tumor selective TRAIL molecules with improved in vivo stability and pharmacokinetic properties, thus reaching an unprecedented potential as tumor therapeutic. 

1. Polypeptide comprising: a) at least three components A, each of which comprises the sequence of a TNF homology domain (THD) of a TNF ligand family member, or a functional derivative thereof, and b) at least one component B consisting of a V_(L) region and a V_(H) region linked directly to each other with a linker sequence L which has a length of ≦12 amino acids.
 2. Polypeptide according to claim 1, wherein the THD of a component A is selected from the group of THD domains consisting of TRAIL, FasL (CD95L), TNF, LT alpha, LT beta, CD30L, CD40L, OX40L, RANKL, TWEAK, LIGHT, CD27L, 4-1 BBL, GITRL, APRIL, EDA, VEGI and BAFF.
 3. Polypeptide according to claim 1, wherein the at least three components A are identical.
 4. Polypeptide according to claim 1, wherein at least one component comprises a sequence selected from the group consisting of SEQ ID NOs: 1-38 or a functional fragment or functional derivative of SEQ ID NOs: 1-38, in particular a functional derivative having at least 80% sequence identity with one of the sequences of SEQ ID NOs: 1-38.
 5. Polypeptide according to claim 1, wherein all at least three components A comprise the sequence of SEQ ID NO: 1 and/or SEQ ID NO:
 5. 6. Polypeptide according claim 1, wherein the at least 3 components A are directly linked to each other via at least two intervening peptide linkers (peptide linker P), preferably wherein a peptide linker P is selected from SEQ ID NOs: 39-91.
 7. Polypeptide according to claim 6, wherein the at least two peptide linkers P are chosen from SEQ ID NOs: 48, 88 and/or
 90. 8. Polypeptide according to claim 1, wherein the V_(L) and V_(H) regions are of an antibody binding to a cell surface molecule selected from the group consisting of: a cytokine receptor, a growth factor receptor, an integrin, a cell adhesion molecule and/or a cell type- or tissue-specific cell surface antigen, cell surface expressed tumor-associated antigens (TAA), and carbohydrates, in particular wherein the V_(L) and V_(H) regions are of an antibody binding to a target antigen selected from the group consisting of: the erbB family of tyrosine kinase receptors (EGFR, HER2, HER3, HER4), VEGFRs, heteromeric integrin α_(x) β_(χ) receptor family, fibroblast activation protein (FAP), galectin, EpCAM, CEA, CD44 and tumor specific variants thereof (CD44v) and other tumor selective cell surface markers, CD2, CD5, CD7, CD19, CD20, CD21, CD22, CD24, CD25, CD30, CD33, CD38, CD40, CD52, CD56, CD71, CD72, CD73, CD105, CD117, CD123, c-Met, PDGFR, IGF1-R, HMW-MAA, TAG-72, GD2, GD3, GM2, folate receptor, Ley, MUC-1, MUC-2, PSMA, PSCA and uPAR.
 9. Polypeptide according to claim 8, wherein the V_(L) region is selected from the group consisting of SEQ ID NOs: 92 and 130-132 and/or wherein the V_(H) region is selected from the group consisting of SEQ ID NOs: 93 and 133-135, preferably the V_(L) region is SEQ ID NO: 92 and/or the V_(H) region is SEQ ID NO:
 93. 10. Polypeptide according to claim 1, wherein the V_(L) and V_(H) region of a component B are linked with a linker sequence L chosen from SEQ ID NOs: 39-51 and 53-78, in particular wherein the linker sequence L is SEQ ID NO:
 50. 11. Polypeptide according to claim 1, wherein component B has the sequence of SEQ ID NO: 94, 136, 137 or 138, preferably of SEQ ID NO:
 94. 12. Polypeptide according to claim 1, wherein the polypeptide comprises a glycosylation motif and/or is glycosylated and/or comprises an albumin binding domain (ABD).
 13. Polypeptide according to claim 1, wherein the polypeptide comprises an albumin binding domain (ABD) located between component A and component B or downstream of component A, preferably at the C-terminal end of the polypeptide.
 14. Polypeptide according to claim 1, wherein the polypeptide comprises the sequence of SEQ ID NO: 103, SEQ ID NO: 107, SEQ ID NO: 102, SEQ ID NO: 125, SEQ ID NO: 126, SEQ ID NO: 127, SEQ ID NO: 128 and/or SEQ ID NO:
 129. 15. Polypeptide comprising the sequence of SEQ ID NOs: 96, 97 or
 98. 16. Nucleic acid encoding for the polypeptides according to claim
 1. 17. Polypeptide complex comprising the polypeptide according to claim
 1. 18. Polypeptide complex according to claim 17, which is a dimeric and/or trimeric complex.
 19. Pharmaceutical composition comprising at least one polypeptide according to claim 1; optionally further comprising at least one pharmaceutically acceptable carrier, adjuvant, and/or vehicle.
 20. A method for treating or diagnosing cancer, autoimmune, or degenerative diseases, comprising administering to a subject in need thereof the polypeptide according to claim
 1. 